Use of compound binding to mSin3B that specifically binds to neuron restrictive silencer factor (NRSF)

ABSTRACT

The present invention identifies a compound which binds to the PAH1 domain of mSin3B that specifically binds to neural restrictive silencer factor NRSF, and uses the compound as a prophylactic and/or a therapeutic for diseases associated with abnormal expression of neural restrictive silencer factor NRSF/REST or abnormal expression of genes targeted by NRSF/REST, such as Huntington&#39;s disease, medulloblastoma and neuropathic pain. 
     The present invention provides a pharmaceutical composition comprising a substance capable of binding to the PAH1 domain of mSin3B, e.g., a compound represented by the following formula (1), a pharmacologically acceptable salt thereof, or a pharmacologically acceptable ester thereof: 
                         
wherein n represents 0 or 1; R 1 , R 2 , R 3 , R 4  and R 5  each independently represent a hydrogen atom, a hydrocarbon group or a functional group; Y represents a single bond, a carbonyl group, —CONH—, —NHCO— or a sulfonyl group; and Z represents a nitrogen-containing heterocyclic group which may have a substituent, an amino group which may have a hydrocarbon group or an aromatic hydrocarbon group, or a nitrogen and oxygen-containing heterocyclic group which may have a substituent.

CROSS REFERENCE TO THE RELATED APPLICATIONS

This application is a national stage of international application No. PCT/JP2011/052710, filed on Feb. 9, 2011 and claims the benefit of priority under 35 USC 119 to Japanese Patent Application No. 2010-027066, filed on Feb. 10, 2010, the entire contents of which are incorporated herein by reference.

TECHNICAL FIELD

The present invention relates to use of compounds binding to mSin3B that specifically binds to a neural restrictive silencer factor (NRSF). More specifically, the present invention relates to medicinal applications of compounds binding to mSin3B that specifically binds to NRSF.

BACKGROUND ART

Formation of normal cells, tissues and organs in the body is achieved through expression of genes at appropriate times, in appropriate places and in appropriate quantities. As a result, normal function is exerted. For example, neural genes must be expressed properly in neuronal cells but not in non-neural cells. NRSE/RE1 (neural restrictive silencer element/repressor element 1) is a silencer consisting of 21 base pairs and present in the vicinity of neuron specific genes. This silencer plays a central role in neuron-specific transcriptional regulation of more than 30 genes for such substances as neurotransmitter synthetases, ion channels, neuronal growth-associated proteins, and so forth. It is said that approximately 1000 genes (mainly neuron specific genes) have this silencer. This silencer does not work in neuronal cells but suppresses expression of neuron specific genes in non-neuronal cells, to thereby assure expression of neuron specific genes in neuronal cells. It is also believed that this silencer is not only involved in the expression control of neuron specific genes but also involved in terminal differentiation of neuronal cells. It is NRSF/REST (neural restrictive silencer factor) that has been identified as a transcriptional repression factor which binds to the above-described NRSE/RE1 and represses expression of neuron specific genes in non-neuronal cells.

It is reported that abnormal expression of NRSF/REST and genes targeted by NRSF/REST is involved in neurodegenerative diseases, such as Down's syndrome, Alzheimer's disease and Huntington's disease, and medulloblastoma.

Down's syndrome is a disease caused by chromosome 21 trisomy mutation. Examination of difference in genes between neural tissues of fetuses dying from Down's syndrome and those of normal fetuses revealed that expression of SCG10 (a neuron-specific growth-associated protein) gene and other genes targeted by NRSF/REST such as decreased greatly in the former. On the other hand, those proteins regulated by transcription factors other than NRSF/REST were expressed normally (Non-Patent Document No. 1).

Alzheimer's disease is a disease caused by accumulation of β amyloid and neurofibrillary tangle and neuronal death. Expression of SCG10 was altered in Alzheimer's disease brains (Non-Patent Document No. 2).

Medulloblastoma is the most malignant brain tumor in children. Expression levels of NRSF/REST in medulloblastoma cells are very high. A recombinant protein REST-VP16 that antagonizes NRSF/REST and activates genes there targeted thereby promotes expression of neuronal genes and also activates the caspase cascade to thereby induce apoptosis. REST-VP16 is a potential therapeutic (Non-Patent Document No. 3).

Huntington's disease is a progressive, neurodegenerative disease manifesting choreic movement, dementia and personality change as major symptoms. It is believed that abnormal huntingtin molecules with a repeat structure of glutamine residues form aggregates to thereby induce neurodegeneration. Wild-type huntingtin binds to NRSF/REST in the cytoplasm to regulate the binding of NRSF/REST to NRSE/RE1. On the other hand, this control is lost in Huntington's disease; thus, neuronal genes are not expressed sufficiently (Non-Patent Document No. 4).

Chronic pain caused by neuronal disorders (neuropathic pain) presents complicated pain symptoms in which positive symptoms (pain hypersensitivity and allodynia (a strong pain induced by a tactile stimulus)) and negative symptoms (hypoesthesia) are mixed. Since this abnormal pain shows resistance to anti-inflammatory drugs and morphine, it is regarded as intractable pain.

Recently, Uchida et al. revealed that expression of the silencer factor NRSF/REST is enhanced in primary sensory neurons after neuropathy to silence a group of pain-associated genes (Na_(v)1.8, MOP, TRPM8, TRPA1 and K_(v)4.3) through epigenetic modification (lowering of histone acetylation) and induce C-fiber hypoesthesia and morphine resistance which are characteristic of neuropathic pain (Non-Patent Documents Nos. 7, 8, 9 and 10).

Further, Naruse et al. revealed that the N-terminal transcriptional repressor domain of NRSF/REST recruits HDAC through co-repressor mSin3 and that the C-terminal transcriptional repressor domain recruits HDAC through CoREST, and suggested that NRSF/REST represses transcription by deactivation of the chromatin structure (Non-Patent Document No. 5).

The present inventors have already analyzed the structure of a complex composed of the N-terminal transcription repressor domain of NRSF (associated with Huntington's disease, medulloblastoma and neuropathic pain) and the PAH1 domain of co-repressor mSin3B which specifically binds to that domain (Patent Document No. 1 and Non-Patent Document No. 6).

However, no compounds have been reported so far which bind to mSin3B that specifically binds to neural restrictive silencer factor NRSF.

DISCLOSURE OF THE INVENTION Problem for Solution by the Invention

It is an object of the present invention to identify compounds which bind to the PAH1 domain of mSin3B that specifically binds to neural restrictive silence factor NRSF that is associated with Huntington's disease, medulloblastoma and neuropathic pain. Such compounds may be used as lead compounds for therapeutics for Huntington's disease, medulloblastoma and neuropathic pain.

Means to Solve the Problem

The present inventors identified by NMR those compounds which bind to the PAH1 domain of mSin3B that specifically binds to neural restrictive silence factor NRSF. Further, the present inventors subjected the above-identified compounds to MTT assay using human medulloblastoma cell strains and found compounds which cause cell death and compounds which inhibit cell growth. Further, hypoesthesia is observed in electrical stimulation-induced paw withdrawal (EPW) test which evaluates pain threshold in response to C-fiber specific electrical stimulation (5 Hz) at the time of neuropathic pain, and disappearance of morphine analgesia is observed in thermal paw withdrawal test which evaluates pain threshold against thermal stimulation. The present inventors found that some of the above-identified compounds that cause recovery from such modulations. The present invention has been achieved based on these findings.

A summary of the present invention is as described below.

-   (1) A pharmaceutical composition comprising a substance capable of     binding to the PAH1 domain of mSin3B. -   (2) The pharmaceutical composition according to (1), wherein the     substance capable of binding to the PAH1 domain of mSin3B is a     compound represented by the following formula (I), a     pharmacologically acceptable salt thereof or a pharmacologically     acceptable ester thereof:

-   -   wherein n represents 0 or 1; R¹, R², R³, R⁴ and R⁵ each         independently represent a hydrogen atom, a hydrocarbon group or         a functional group; Y represents a single bond, a carbonyl         group, —CONH—, —NHCO— or a sulfonyl group; and Z represents a         nitrogen-containing heterocyclic group which may have a         substituent, an amino group which may have a hydrocarbon group         or an aromatic hydrocarbon group, or a nitrogen and         oxygen-containing heterocyclic group which may have a         substituent.

-   (3) The pharmaceutical composition according to (1) or (2), which is     used as a prophylactic and/or a therapeutic for diseases associated     with abnormal expression of neural restrictive silencer factor     NRSF/REST or abnormal expression of genes targeted by NRSF/REST.

-   (4) The pharmaceutical composition according to (3), wherein the     disease associated with abnormal expression of neural restrictive     silencer factor NRSF/REST or abnormal expression of genes targeted     by NRSF/REST is neurodegenerative disease, cancer, atopic     dermatitis, diabetes, cardiomyopathy or neuropathic pain.

-   (5) The pharmaceutical composition according to (4), wherein the     neurodegenerative disease is Down's syndrome, Alzheimer's disease,     Huntington's disease or Parkinson's disease.

-   (6) The pharmaceutical composition according to (4), wherein the     cancer is medulloblastoma.

-   (7) The pharmaceutical composition according to any one of (1) to     (6), wherein the compound represented by formula (I) is represented     by any of the following formulas:

-   (8) A method of preventing and/or treating diseases associated with     abnormal expression of neural restrictive silencer factor NRSF/REST     or abnormal expression of genes targeted by NRSF/REST, comprising     administering to a subject a pharmacologically effective amount of a     substance capable of binding to the PAH1 domain of mSin3B. -   (9) Use of a substance capable of binding to the PAH1 domain of     mSin3B, for preparing a prophylactic and/or a therapeutic for     diseases associated with abnormal expression of neural restrictive     silencer factor NRSF/REST or abnormal expression of genes targeted     by NRSF/REST. -   (10) Use of a substance capable of binding to the PAH1 domain of     mSin3B, for preventing and/or treating diseases associated with     abnormal expression of neural restrictive silencer factor NRSF/REST     or abnormal expression of genes targeted by NRSF/REST. -   (11) A substance capable of binding to the PAH1 domain of mSin3B,     for use in a method of preventing and/or treating diseases     associated with abnormal expression of neural restrictive silencer     factor NRSF/REST or abnormal expression of genes targeted by     NRSF/REST. -   (12) A compound represented by the following formula (Ia), a     pharmacologically acceptable salt thereof, or a pharmacologically     acceptable ester thereof

-   -   wherein n_(a) represents 0 or 1; R_(a) ¹, R_(a) ², R_(a) ³,         R_(a) ⁴ and R_(a) ⁵ each independently represent a hydrogen         atom, a hydrocarbon group or a functional group; Y_(a)         represents a single bond, a carbonyl group, —CONH—, —NHCO— or a         sulfonyl group; and Z_(a) represents a nitrogen-containing         heterocyclic group which may have a substituent, an amino group         which may have a hydrocarbon group or an aromatic hydrocarbon         group, or a nitrogen and oxygen-containing heterocyclic group         which may have a substituent.

-   (13) The compound, the pharmacologically acceptable salt thereof or     the pharmacologically acceptable ester thereof according to (8),     wherein the compound represented by formula (Ia) is a compound     represented by any of the following formulas:

Effect of the Invention

Substances capable of binding to the PAH1 domain of mSin3B (for example, compounds represented by formula (I), pharmacologically acceptable salts thereof, or pharmacologically acceptable esters thereof) may be used as a medicine, in particular, a prophylactic and/or a therapeutic for diseases associated with abnormal expression of neural restrictive silencer factor NRSF/REST or abnormal expression of genes targeted by NRSF/REST.

The present specification encompasses the contents disclosed in the specification and/or the drawings of Japanese Patent Application No. 2010-27066 based on which the present application claims priority.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the STD (saturation transfer difference) of 3,5-dimethylpiperidyl 3-methyl-4-nitrophenyl ketone (compound/mSin3B: 400 μM/10 μM).

FIG. 2 shows the STD (saturation transfer difference) of 1-[4-(difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one (compound/mSin3B: 400 μM/10 μM).

FIG. 3 shows the STD (saturation transfer difference) of compound 5 (3,5-dimethylpiperidyl 4-chloro-3-nitrophenyl ketone) (compound/mSin3B: 400 μM/10 μM).

FIG. 4 shows the STD (saturation transfer difference) of compound 15 (3,5-dimethylpiperidyl 4-fluorophenyl ketone) (compound/mSin3B: 400 μM/10 μM).

FIG. 5 shows the STD (saturation transfer difference) of compound 23 (2-(2,6-dimethylmorpholin-4-yl)-N-(2-chloro-4-fluorophenyl)acetamide) (compound/mSin3B: 400 μM/10 μM).

FIG. 6 shows the STD (saturation transfer difference) of compound NCR6 (1-benzoyl-3,5-dimethylpiperidine) (compound/mSin3B: 400 μM/10 μM).

FIG. 7 shows the STD (saturation transfer difference) of compound NCR7 (3,5-dimethyl-1-(3-methyl-4-nitrobenzyl)piperidine) (compound/mSin3B: 400 μM/10 μM).

FIG. 8 shows the STD (saturation transfer difference) of compound NCR11 (3,5-dimethyl-1-(4-chlorobenzoyl)piperidine) (compound/mSin3B: 400 μM/10 μM).

FIG. 9 shows the STD (saturation transfer difference) of compound NCR13 (3-methyl-4-nitro-N,N-dipropylbenzamide) (compound/mSin3B: 400 μM/10 μM).

FIG. 10 shows the STD (saturation transfer difference) of compound NCR14 (N,N-diisobutyl-3-methyl-4-nitrobenzamide) (compound/mSin3B: 400 μM/10 μM).

FIG. 11 shows the STD (saturation transfer difference) of compound NCR15 (N,N-diisopropyl-3-methyl-4-nitrobenzamide) (compound/mSin3B: 400 μM/10 μM).

FIG. 12 shows the dose dependency of compounds 5, 15 and 23 (100 μg/ml) in their growth inhibition activities against human medulloblastoma cells.

FIG. 13 shows the growth inhibition activities of compounds NCR6, 7, 11, 13, 14 and 15 (200 μM and 20 μM) against human medulloblastoma cells.

FIG. 14 shows the results of analysis of mRNA levels of pain-associated genes (Na_(v)1.8 and MOP) in dorsal root ganglia at 3, 6 and 12 hours after a single administration of mSin3B compound (A28) 3 days after nerve injury (n=3).

FIG. 15 shows the results of evaluation with EPW test of the efficacies of mSin3B compounds (A28, 155 and 106 (NC)) (0.5 nmol i.t.) against hypoesthesia after nerve injury.

FIG. 16 shows the results of analysis of the effects of mSin3B compounds (A28 and 155) on pain threshold when they were systemically (intraperitoneally) administered (5 mg/kg) consecutively on day 3, 4 and 5 after injury.

FIG. 17 shows the results of evaluation with thermal paw withdrawal test of the efficacies of mSin3B compounds (A28, 155 and 106 (NC)) (0.5 nmol i.t.) against morphine resistance after nerve injury.

FIG. 18 shows the results of evaluation by a quantitative real time method of mRNA levels of Na_(v)1.8 in dorsal root ganglia after administration of mSin3B compounds (A28 and 155) (0.5 nmol i.t.).

BEST MODES FOR CARRYING OUT THE INVENTION

Hereinbelow, modes for carrying out the present invention will be described in more detail.

The present invention provides a pharmaceutical composition comprising a substance capable of binding to the PAH1 domain of mSin3B. Specific examples of the substance capable of binding to the PAH1 domain of mSin3B include, but are not limited to, compounds represented by the following formula (I), pharmacologically acceptable salts thereof, and pharmacologically acceptable esters thereof.

wherein n represents 0 or 1; R¹, R², R³, R⁴ and R⁵ each independently represent a hydrogen atom, a hydrocarbon group or a functional group; Y represents a single bond, a carbonyl group, —CONH—, —NHCO— or a sulfonyl group; and Z represents a nitrogen-containing heterocyclic group which may have a substituent, an amino group which may have a hydrocarbon group or an aromatic hydrocarbon group, or a nitrogen and oxygen-containing heterocyclic group which may have a substituent.

As the hydrocarbon group of R¹, R², R⁴ and R⁵ specific examples include, but are not limited to, alkyl groups (preferably, C₁-C₆ straight-chained or branched alkyl groups, more preferably, methyl group, ethyl group, normal propyl group, isopropyl group, etc.).

As the functional group of R¹, R², R⁴ and R⁵, specific examples include, but are not limited to, alkoxy groups (preferably, C₁-C₆ straight-chained or branched alkoxy groups, more preferably, methoxy group, ethoxy group, etc.), sulfonyl group which may have a substituent, nitro group, halogen groups (fluoro group, chloro group, bromo group, iodo group, etc.), and sulfamoyl group which may have a substituent. As the substituents on sulfonyl group and sulfamoyl group, specific examples include, but are not limited to, those substituents listed in Tables provided herein later.

As the hydrocarbon group of R³, specific examples include, but are not limited to, aromatic hydrocarbon groups (preferably, C₁-C₆ aromatic hydrocarbon groups, more preferably, phenyl, naphthyl, anthryl, phenanthryl, acenaphthylenyl, biphenylyl, indenyl, etc.), alkyl groups which may have a substituent (preferably, C₁-C₆ straight-chained or branched alkyl groups, more preferably, methyl group, ethyl group, normal propyl group, isopropyl group, normal butyl group, isobutyl group, s-butyl group, t-butyl group, etc.), and alkenyl groups which may have a substituent (preferably, C₂-C₆ straight-chained or branched alkenyl groups, more preferably, vinyl group and 1-isopropenyl group). As the substituent on alkyl groups and alkenyl groups, specific examples include, but are not limited to, those substituents listed in Tables provided herein later.

As the functional group of R³, specific examples include, but are not limited to, nitro group, difluoromethoxy group, amide groups which may have a substituent, halogen groups (fluoro group, chloro group, bromo group, iodo group, etc.), alkoxy group which may have a substituent (preferably, C₁-C₆ straight-chained or branched alkoxy groups, more preferably, methoxy group, ethoxy group, propoxy group, isopropoxy group, butoxy group, isobutoxy group, s-butoxy group, t-butoxy group, pentyloxy group, hexyloxy group, etc.), acetoxy group, cyano group, sulfonyl group which may have a substituent, sulfamoyl group which may have a substituent, amino groups which may have a substituent, piperidyl group which may have a substituent, phenoxy group, hydroxy group, acyl groups, triazolyl group, imidazolyl group, alkoxycarbonyl groups (wherein the alkoxy group is preferably a C₁-C₆ straight-chained or branched alkoxy group, more preferably, methoxy group or ethoxy group), tetrazolyl group, pyrazolyl group which may have a substituent, piperidylcarbonyl group which may have a substituent, pyrrolidinyl group, alkylsulfanyl groups which may have a substituent (wherein the alkyl group is preferably a C₁-C₆ straight-chained or branched alkyl groups, more preferably, methyl group, ethyl group, normal propyl group, isopropyl group, normal butyl group, isobutyl group, s-butyl group, t-butyl group, etc.), oxadiazolyl group which may have a substituent, and heterocyclic groups which may have a substituent (wherein the heterocyclic group is preferably a 5-10 membered heterocyclic group containing 1-3 heteroatoms (e.g., sulfur atom, oxygen atom, nitrogen atom, etc.), more preferably 3H-quinazoline-4-one, 2,4,5-trihydroisothiazole-1,1,3-trione, benzoimidazole and the like). As the substituent in amide groups, alkoxy groups, sulfonyl group, sulfamoyl group, amino groups, piperidyl group, pyrazolyl group, piperidylcarbonyl group, alkylsulfanyl groups, oxadiazolyl group and heterocyclic groups, and as the acyl group, specific examples include, but are not limited to, those listed in Tables provided herein later.

As the “substituent” in the “nitrogen-containing heterocyclic group which may have a substituent” in Z, specific examples include, but are not limited to, saturated chain hydrocarbon groups (e.g., C₁-C₆ alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, neopentyl, t-pentyl, 1-methylbutyl and hexyl), unsaturated chain hydrocarbon groups (e.g., C₂-C₆ alkenyl groups such as vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl and 3-methylallyl; and C₂-C₆ alkynyl groups such as ethynyl and 2-propynyl), alicyclic hydrocarbon groups (such as cyclohexyl, 1-cyclohexenyl and cyclohexylidene), and aromatic hydrocarbon groups (such as benzyl, tolyl and xylyl). The number of such substituent may be one or more.

As the “nitrogen-containing heterocyclic group” in the “nitrogen-containing heterocyclic group which may have a substituent” in Z, specific examples include, but are not limited to, nitrogen-containing 3-8 membered rings such as aziridine, azetidine, pyrrolidine, piperidine, hexamethyleneimine and heptamethyleneimine.

As the “hydrocarbon group” in the “amino group which may have a hydrocarbon group or an aromatic hydrocarbon group” in Z, specific examples include, but are not limited to, saturated chain hydrocarbon groups (e.g., C₁-C₆ alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, neopentyl, t-pentyl, 1-methylbutyl and hexyl), unsaturated chain hydrocarbon groups (e.g., C₂-C₆ alkenyl groups such as vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl and 3-methylallyl; and C₂-C₆ alkynyl groups such as ethynyl and 2-propynyl), and alicyclic hydrocarbon groups (such as cyclohexyl, 1-cyclohexenyl and cyclohexylidene). As the aromatic hydrocarbon group, such as benzyl, tolyl, xylyl and the like may be given. The amino group may have one or more hydrocarbon groups and/or aromatic hydrocarbon groups.

As the “substituent” in the “nitrogen and oxygen-containing heterocyclic group which may have a substituent” in Z, specific examples include, but are not limited to, saturated chain hydrocarbon groups (e.g., C₁-C₆ alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, neopentyl, t-pentyl, 1-methylbutyl and hexyl), unsaturated chain hydrocarbon groups (e.g., C₂-C₆ alkenyl groups such as vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl and 3-methylallyl; and C₂-C₆ alkynyl groups such as ethynyl and 2-propynyl), alicyclic hydrocarbon groups (such as cyclohexyl, 1-cyclohexenyl and cyclohexylidene), and aromatic hydrocarbon groups (such as benzyl, tolyl and xylyl). The number of such substituent may be one or more.

As the “nitrogen and oxygen-containing heterocyclic group” in the “nitrogen and oxygen-containing heterocyclic group which may have a substituent” in Z, specific examples include, but are not limited to, morpholine.

Specific examples of the compound represented by formula (I) include, but are not limited to, 3,5-dimethylpiperidyl 3-methyl-4-nitrophenyl ketone, 1-[4-(difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one, 3,5-dimethylpiperidyl 4-chloro-3-nitrophenyl ketone, 3,5-dimethylpiperidyl 4-fluorophenyl ketone, (2-(2,6-dimethylmorpholin-4-yl)-N-(2-chloro-4-fluorophenyl)acetamide and 3,5-dimethyl-1-(3-methyl-4-nitrobenzyl)piperidine). The structures of 3,5-dimethylpiperidyl 3-methyl-4-nitrophenyl ketone (compound 155), 1-[4-(difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one (compound A28), 3,5-dimethylpiperidyl 4-chloro-3-nitrophenyl ketone (compound 5), 3,5-dimethylpiperidyl 4-fluorophenyl ketone (compound 15), 2-(2,6-dimethylmorpholin-4-yl)-N-(2-chloro-4-fluorophenyl)acetamide (compound 23) and 3,5-dimethyl-1-(3-methyl-4-nitrobenzyl)piperidine (compound NCR7) are described below.

3,5-Dimethylpiperidyl 3-methyl-4-nitrophenyl ketone may be purchased from SPECS (Netherland), Asinex Gold (Russia) or ASDI (U.S.A.).

1-[4-(Difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one may be purchased from Enamine (Ukraine).

Compound 5 may be purchased from Vitas-M Laboratory, Ltd. (Russia).

Compound 15 may be purchased from Vitas-M Laboratory, Ltd. (Russia).

Compound 23 may be purchased from Enamine (Ukraine).

Compound NCR-7 may be prepared according to the method described in Preparation Example 21.

It should be noted that the compound represented by formula (I) may be a compound represented by the following formula (Ia).

wherein n_(a) represents 0 or 1; R_(a) ¹, R_(a) ², R_(a) ³, R_(a) ⁴ and R_(a) ⁵ each independently represent a hydrogen atom, a hydrocarbon group or a functional group; Y_(a) represents a single bond, a carbonyl group, —CONH—, —NHCO— or a sulfonyl group; and Z_(a) represents a nitrogen-containing heterocyclic group which may have a substituent, an amino group which may have a hydrocarbon group or an aromatic hydrocarbon group, or a nitrogen and oxygen-containing heterocyclic group which may have a substituent.

As the hydrocarbon group of R_(a) ¹, R_(a) ², R_(a) ⁴, and R_(a) ⁵, specific examples include, but are not limited to, alkyl groups (preferably, C₁-C₆ straight-chained or branched alkyl groups, more preferably, methyl group, ethyl group, normal propyl group, isopropyl group, etc.).

As the functional group of R_(a) ¹, R_(a) ², R_(a) ⁴, and R_(a) ⁵, specific examples include, but are not limited to, alkoxy groups (preferably, C₁-C₆ straight-chained or branched alkoxy groups, more preferably, methoxy group, ethoxy group, etc.), sulfonyl group which may have a substituent, nitro group, halogen groups (fluoro group, chloro group, bromo group, iodo group, etc.), and sulfamoyl group which may have a substituent. As the substituents in sulfonyl group and sulfamoyl group, specific examples include, but are not limited to, those substituents listed in Tables provided herein later.

As the hydrocarbon group of R_(a) ³, specific examples include, but are not limited to, aromatic hydrocarbon groups (preferably, C₆-C₁₄ aromatic hydrocarbon groups, more preferably, phenyl, naphthyl, anthryl, phenanthryl, acenaphthylenyl, biphenylyl, indenyl, etc.), alkyl groups which may have a substituent (preferably, C₁-C₆ straight-chained or branched alkyl groups, more preferably, methyl group, ethyl group, normal propyl group, isopropyl group, normal butyl group, isobutyl group, s-butyl group, t-butyl group, etc.), and alkenyl groups which may have a substituent (preferably, C₂-C₆ straight-chained or branched alkenyl groups, more preferably, vinyl group and 1-isopropenyl group). As the substituent in alkyl groups and alkenyl groups, specific examples include, but are not limited to, those substituents listed in Tables provided herein later.

As the functional group of R_(a) ³, specific examples include, but are not limited to, nitro group, difluoromethoxy group, amide groups which may have a substituent, halogen groups (fluoro group, chloro group, bromo group, iodo group, etc.), alkoxy group which may have a substituent (preferably, C₁-C₆ straight-chained or branched alkoxy groups, more preferably, methoxy group, ethoxy group, propoxy group, isopropoxy group, butoxy group, isobutoxy group, s-butoxy group, t-butoxy group, pentyloxy group, hexyloxy group, etc.), acetoxy group, cyano group, sulfonyl group which may have a substituent, sulfamoyl group which may have a substituent, amino groups which may have a substituent, piperidyl group which may have a substituent, phenoxy group, hydroxy group, acyl groups, triazolyl group, imidazolyl group, alkoxycarbonyl groups (wherein the alkoxy group is preferably a C₁-C₆ straight-chained or branched alkoxy group, more preferably, methoxy group or ethoxy group), tetrazolyl group, pyrazolyl group which may have a substituent, piperidylcarbonyl group which may have a substituent, pyrrolidinyl group, alkylsulfanyl groups which may have a substituent (wherein the alkyl group is preferably a C₁-C₆ straight-chained or branched alkyl groups, more preferably, methyl group, ethyl group, normal propyl group, isopropyl group, normal butyl group, isobutyl group, s-butyl group, t-butyl group, etc.), oxadiazolyl group which may have a substituent, and heterocyclic groups which may have a substituent (wherein the heterocyclic group is preferably a 5-10 membered heterocyclic group containing 1-3 heteroatoms (e.g., sulfur atom, oxygen atom, nitrogen atom, etc.), more preferably 3H-quinazoline-4-one, 2,4,5-trihydroisothiazole-1,1,3-trione, benzoimidazole and the like). As the substituent in amide groups, alkoxy groups, sulfonyl group, sulfamoyl group, amino groups, piperidyl group, pyrazolyl group, piperidylcarbonyl group, alkylsulfanyl groups, oxadiazolyl group and heterocyclic groups; and the acyl group, specific examples include, but are not limited to, those listed in Tables provided herein later.

As the “substituent” in the “nitrogen-containing heterocyclic group which may have a substituent” in Z_(a), specific examples include, but are not limited to, saturated chain hydrocarbon groups (e.g., C₁-C₆ alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, neopentyl, t-pentyl, 1-methylbutyl and hexyl), unsaturated chain hydrocarbon groups (e.g., C₂-C₆ alkenyl groups such as vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl and 3-methylallyl; and C₂-C₆ alkynyl groups such as ethynyl and 2-propynyl), alicyclic hydrocarbon groups (such as cyclohexyl, 1-cyclohexenyl and cyclohexylidene), and aromatic hydrocarbon groups (such as benzyl, tolyl and xylyl). The number of such substituent may be one or more.

As the “nitrogen-containing heterocyclic group” in the “nitrogen-containing heterocyclic group which may have a substituent” in Z_(a), specific examples include, but are not limited to, nitrogen-containing 3-8 membered rings such as aziridine, azetidine, pyrrolidine, piperidine, hexamethyleneimine and heptamethyleneimine.

As the “hydrocarbon group” in the “amino group which may have a hydrocarbon group or an aromatic hydrocarbon group” in Z_(a), specific examples include, but are not limited to, saturated chain hydrocarbon groups (e.g., C₁-C₆ alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, neopentyl, t-pentyl, 1-methylbutyl and hexyl), unsaturated chain hydrocarbon groups (e.g., C₂-C₆ alkenyl groups such as vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl and 3-methylallyl; and C₂-C₆ alkynyl groups such as ethynyl and 2-propynyl), and alicyclic hydrocarbon groups (such as cyclohexyl, 1-cyclohexenyl and cyclohexylidene). As the aromatic hydrocarbon group, such as benzyl, tolyl, xylyl and the like may be given. The amino group may have one or more hydrocarbon groups and/or aromatic hydrocarbon groups.

As the “substituent” in the “nitrogen and oxygen-containing heterocyclic group which may have a substituent” in Z_(a), specific examples include, but are not limited to, saturated chain hydrocarbon groups (e.g., C₁-C₆ alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, neopentyl, t-pentyl, 1-methylbutyl and hexyl), unsaturated chain hydrocarbon groups (e.g., C₂-C₆ alkenyl groups such as vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl and 3-methylallyl; and C₂-C₆ alkynyl groups such as ethynyl and 2-propynyl), alicyclic hydrocarbon groups (such as cyclohexyl, 1-cyclohexenyl and cyclohexylidene), and aromatic hydrocarbon groups (such as benzyl, tolyl and xylyl). The number of such substituent may be one or more.

As the “nitrogen and oxygen-containing heterocyclic group” in the “nitrogen and oxygen-containing heterocyclic group which may have a substituent” in Z_(a), specific examples include, but are not limited to, morpholine.

Those compounds represented by formula (Ia) may be prepared according to any of the methods disclosed in Schemes 1 to 4 in Preparation Examples provided later, or according to the method with necessary modifications.

The present invention also provides compounds represented by formula (Ia), pharmacologically acceptable salts thereof or pharmacologically acceptable ester thereof.

As specific examples of the compound represented by formula (Ia), those compounds represented by any of the following formulas may be given.

Commercially available compounds which are represented by formula (I) (excluding 3,5-dimethylpiperidyl 3-methyl-4-nitrophenyl ketone and 1-[4-(difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one) are listed in the Tables below.

TABLE 1 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 1 Zelinsky UZI/1846284 N-{4-[(3,5- 0 H H (ART-CHEM) dimethylpiperidyl)carbonyl]phenyl} (Germany) butanamide 1 Vitas-M STK167991 N-{4-[(3,5- 0 H H (Russia) dimethylpiperidyl)carbonyl]phenyl} butanamide 2 Zelinsky UZI/6203309 3,5-dimethylpiperidyl 0 H H (ART-CHEM) 4-chlorophenyl ketone (Germany) 2 Vitas-M STK064998 3,5-dimethylpiperidyl 0 H H (Russia) 4-chlorophenyl ketone 3 Zelinsky UZI/7104337 3,5-dimethylpiperidyl 0 H H (ART-CHEM) 4-ethoxyphenyl ketone (Germany) 3 Vitas-M STK089384 3,5-dimethylpiperidyl 0 H H (Russia) 4-ethoxyphenyl ketone 4 Zelinsky UZI/8010939 3,5-dimethylpiperidyl 0 H H (ART-CHEM) 4-phenylphenyl ketone (Germany) 4 Vitas-M STK128213 3,5-dimethylpiperidyl 0 H H (Russia) 4-phenylphenyl ketone Sample Chemical Molecular No R³ Formula Weight 1 NHCO(CH₂)₂CH₃ C₁₈H₂₆N₂O₂ 302.41 1 NHCO(CH₂)₂CH₃ C₁₈H₂₆N₂O₂ 302.41 2 Cl C₁₄H₁₈ClNO 251.75 2 Cl C₁₄H₁₈ClNO 251.75 3 OCH₂CH₃ C₁₆H₂₃NO₂ 261.36 3 OCH₂CH₃ C₁₆H₂₃NO₂ 261.36 4 C₆H₅ C₂₀H₂₃NO 293.4 4 C₆H₅ C₂₀H₂₃NO 293.4

TABLE 2 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 5 ENAMINE T6039603 3,5-dimethylpiperidyl 0 H NO₂ (Ukraine) 4-methoxy-3-nitrophenyl ketone 5 Vitas-M STK099651 3,5-dimethylpiperidyl 0 H NO₂ (Russia) 4-methoxy-3-nitrophenyl ketone 6 Zelinsky UZI/8022038 3,4-dimethylphenyl 0 H CH₃ (ART-CHEM) 3,5-dimethylpiperidyl ketone (Germany) 7 Zelinsky UZI/8037813 3,5-dimethylpiperidyl 0 H H (ART-CHEM) 4-methoxyphenyl ketone (Germany) 7 Vitas-M STK008245 3,5-dimethylpiperidyl 0 H H (Russia) 4-methoxyphenyl ketone 8 Zelinsky UZI/8062904 3,4-dichlorophenyl 0 H Cl (ART-CHEM) 3,5-dimethylpiperidyl ketone (Germany) 8 Vitas-M STK019928 3,4-dichlorophenyl 0 H Cl (Russia) 3,5-dimethylpiperidyl ketone 9 Zelinsky UZI/8075653 3,5-dimethylpiperidyl 0 H H (ART-CHEM) 4-fluorophenyl ketone (Germany) 9 Vitas-M STK036338 3,5-dimethylpiperidyl 0 H H (Russia) 4-fluorophenyl ketone Chemical Molecular Sample No R³ Formula Weight 5 OCH₃ C₁₅H₂₀N₂O₄ 292.33 5 OCH₃ C₁₅H₂₀N₂O₄ 292.33 6 CH₃ C₁₆H₂₃NO 245.36 7 OCH₃ C₁₅H₂₁NO₂ 247.33 7 OCH₃ C₁₅H₂₁NO₂ 247.33 8 Cl C₁₄H₁₇Cl₂NO 286.2 8 Cl C₁₄H₁₇Cl₂NO 286.2 9 F C₁₄H₁₈FNO 235.3 9 F C₁₄H₁₈FNO 235.3

TABLE 3 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 10 Zelinsky UZI/8077610 3,5-dimethylpiperidyl 4-chloro- 0 H NO₂ (ART-CHEM) 3-nitrophenyl ketone (Germany) 10 Vitas-M STK072980 3,5-dimethylpiperidyl 4-chloro- 0 H NO₂ (Russia) 3-nitrophenyl ketone 11 Vitas-M STK039793 3,5-dimethylpiperidyl 4- 0 H H (Russia) methylphenyl ketone 12 Vitas-M STK038754 3,5-dimethylpiperidyl 4- 0 H H (Russia) bromophenyl ketone 12 AsinexGold BAS 3,5-dimethylpiperidyl 4- 0 H H (Russia) 00623311 bromophenyl ketone 13 Zelinsky UZI/8109564 N-{4-[(3,5dimethylpiperidyl) 0 H H (ART-CHEM) carbonyl]phenyl}acetamide (Germany) 13 Vitas-M STK001156 N-{4-[(3,5-dimethylpiperidyl) 0 H H (Russia) carbonyl]phenyl}acetamide 14 TimTec ST008578 4-[(3,5-dimethylpiperidyl)carbonyl] 0 H H (USA) phenyl acetate Chemical Molecular Sample No R³ Formula Weight 10 Cl C₁₄H₁₇ClN₂O₃ 296.75 10 Cl C₁₄H₁₇ClN₂O₃ 296.75 11 CH₃ C₁₅H₂₁NO 231.33 12 Br C₁₄H₁₈BrNO 296.2 12 Br C₁₄H₁₈BrNO 296.2 13 NHCOCH₃ C₁₆H₂₂N₂O₂ 274.36 13 NHCOCH₃ C₁₆H₂₂N₂O₂ 274.36 14 OCOCH₃ C₁₆H₂₁NO₃ 275.34

TABLE 4 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 15 ENAMINE T6039629 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-nitrophenyl ketone 15 Vitas-M STK057760 3,5-dimethylpiperidyl 0 H H (Russia) 4-nitrophenyl ketone 16 Zelinsky UZI/8144985 3,5-dimethylpiperidyl 0 H NO₂ (ART-CHEM) 4-methyl-3-nitrophenyl ketone (Germany) 16 Vitas-M STK100255 3,5-dimethylpiperidyl 0 H NO₂ (Russia) 4-methyl-3-nitrophenyl ketone 17 Zelinsky UZI/8147502 4-(tert-butyl)phenyl 0 H H (ART-CHEM) 3,5-dimethylpiperidyl ketone (Germany) 17 Vitas-M STK081887 4-(tert-butyl)phenyl 0 H H (Russia) 3,5-dimethylpiperidyl ketone 18 Zelinsky UZI/8160409 3,5-dimethylpiperidyl 0 OCH₃ OCH₃ (ART-CHEM) 3,4,5-trimethoxyphenyl ketone (Germany) 18 AsinexGold BAS 3,5-dimethylpiperidyl 0 OCH₃ OCH₃ (Russia) 01130446 3,4,5-trimethoxyphenyl ketone Chemical Molecular Sample No R³ Formula Weight 15 NO₂ C₁₄H₁₈N₂O₃ 262.3 15 NO₂ C₁₄H₁₈N₂O₃ 262.3 16 CH₃ C₁₅H₂₀N₂O₃ 276.33 16 CH₃ C₁₅H₂₀N₂O₃ 276.33 17 C(CH₃)₃ C₁₈H₂₇NO 273.41 17 C(CH₃)₃ C₁₈H₂₇NO 273.41 18 OCH₃ C₁₇H₂₅NO₄ 307.38 18 OCH₃ C₁₇H₂₅NO₄ 307.38

TABLE 5 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 19 SPECS AF- 3,5-dimethylpiperidyl 0 H H (Netherlands) 399/41895463 4-hexyloxyphenyl ketone 19 Princeton OSSK_288718 3,5-dimethylpiperidyl 0 H H (USA) 4-hexyloxyphenyl ketone 19 ASDI 950015532 3,5-dimethylpiperidyl 0 H H (USA) 4-hexyloxyphenyl ketone 20 Zelinsky UZI/2314952 N-{4-[(3,5-dimethylpiperidyl) 0 H H (ART-CHEM) carbonyl]phenyl}propanamide (Germany) 20 Vitas-M STK204680 N-{4-[(3,5-dimethylpiperidyl) 0 H H (Russia) carbonyl]phenyl}propanamide 21 Vitas-M STK131260 N-{4-[(3,5dimethylpiperidyl) 0 H H (Russia) carbonyl]phenyl}- 2-methylpropanamide 21 Princeton OSSK_802625 N-{4-[(3,5-dimethylpiperidyl) 0 H H (USA) carbonyl]phenyl}- 2-methylpropanamide Chemical Molecular Sample No R³ Formula Weight 19 O(CH₂)₅CH₃ C₂₀H₃₁NO₂ 317.47 19 O(CH₂)₅CH₃ C₂₀H₃₁NO₂ 317.47 19 O(CH₂)₅CH₃ C₂₀H₃₁NO₂ 317.47 20 NHCOCH₂CH₃ C₁₇H₂₄N₂O₂ 288.38 20 NHCOCH₂CH₃ C₁₇H₂₄N₂O₂ 288.38 21 NHCOCH(CH₃)₂ C₁₈H₂₆N₂O₂ 302.41 21 NHCOCH(CH₃)₂ C₁₈H₂₆N₂O₂ 302.41

TABLE 6 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 22 AsinexGold BAS 3,4-dimethoxyphenyl 0 H OCH₃ (Russia) 00783988 3,5-dimethylpiperidyl ketone 22 SPECS AK- 3,4-dimethoxyphenyl 0 H OCH₃ (Netherlands) 968/11658636 3,5-dimethylpiperidyl ketone 22 ASDI 250005641 3,4-dimethoxyphenyl 0 H OCH₃ (USA) 3,5-dimethylpiperidyl ketone 23 Chem T&I NSB 0011060 3,5-dimethylpiperidyl 0 H H (Russia) 4-(methylethyl)phenyl ketone 24 Chem T&I NSB 0014060 3,5-dimethylpiperidyl 0 OCH₂CH₃ OCH₂CH₃ (Russia) 3,4,5-triethoxyphenyl ketone 25 LifeChemicals F0412-0136 4-[(3,5-dimethylpiperidyl) 0 H H (Ukraine) carbonyl]benzenecarbonitrile 26 ENAMINE T0517-3789 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-(trifluoromethyl)phenyl ketone 27 ENAMINE T6086857 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-(pyrrolidinylsulfonyl) phenyl ketone Chemical Molecular Sample No R³ Formula Weight 22 OCH₃ C₁₆H₂₃NO₃ 277.36 22 OCH₃ C₁₆H₂₃NO₃ 277.36 22 OCH₃ C₁₆H₂₃NO₃ 277.36 23 CH(CH₃)₂ C₁₇H₂₅NO 259.39 24 OCH₂CH₃ C₂₀H₃₁NO₄ 349.46 25 CN C₁₅H₁₈N₂O 242.32 26 CF₃ C₁₅H₁₈F₃NO 285.3 27

C₁₈H₂₆N₂O₃S 350.48

TABLE 7 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 27 UOS PB327301926 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-(pyrrolidinylsulfonyl)phenyl ketone 28 LifeChemicals F0412-0130 4-[(dimethylamino)sulfonyl]phenyl 0 H H (Ukraine) 3,5-dimethylpiperidyl ketone 29 ENAMINE EN400-09530 4-(aminomethyl)phenyl 0 H H (Ukraine) 3,5-dimethylpiperidyl ketone 30 ENAMINE T5677980 3,5-dimethylpiperidyl 0 H NO₂ (Ukraine) 3-nitro-4-piperidylphenyl ketone 31 ENAMINE T5715818 3,5-dimethylpiperidyl 4-(4- 0 H NO₂ (Ukraine) methylpiperidyl)- 3-nitrophenyl ketone 32 ENAMINE T5875122 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-phenoxyphenyl ketone 33 Princeton OSSK_810095 3,5-dimethylpiperidyl 4- 0 H H (USA) [(4-chloropyrazolyl)methyl]phenyl ketone 34 ENAMINE T6184998 3,5-dimethylpiperidyl 3-chloro- 0 H Cl (Ukraine) 4-hydroxyphenyl ketone 35 Vitas-M STK296851 N-{4-[(3,5-dimethylpiperidyl) 0 H H (Russia) carbonyl]phenyl}benzamide 35 Princeton OSSK_926474 N-{4-[(3,5-dimethylpiperidyl) 0 H H (USA) carbonyl]phenyl}benzamide Chemical Molecular Sample No R³ Formula Weight 27

C₁₈H₂₆N₂O₃S 350.48 28 SO₂N(CH₃)₂ C₁₆H₂₄N₂O₃S 324.44 29 CH₂NH₂ C₁₅H₂₂N₂O 246.35 30

C₁₉H₂₇N₃O₃ 345.44 31

C₂₀H₂₉N₃O₃ 359.46 32

C₂₀H₂₃NO₂ 309.4 33

C₁₈H₂₂ClN₃O 331.84 34 OH C₁₄H₁₈ClNO₂ 267.75 35

C₂₁H₂₄N₂O₂ 336.43 35

C₂₁H₂₄N₂O₂ 336.43

TABLE 8 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 36 Chem T&I SER/0141547 N-{4-[(3,5- 0 H H (Russia) dimethylpiperidyl)carbonyl]phenyl} (4-methylphenyl)carboxamide 37 Chem T&I SER/0141838 N-{4-[(3,5- 0 H H (Russia) dimethylpiperidyl)carbonyl]phenyl}- 2-furylcarboxamide 38 ENAMINE T5989827 3,5-dimethylpiperidyl 3-methoxy- 0 OCH₃ H (Ukraine) 4-(phenylmethoxy)phenyl ketone 39 ENAMINE T6124051 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-(phenylcarbonyl)phenyl ketone 40 Princeton OSSK_931623 3,5-dimethylpiperidyl 0 H H (USA) 4-[(prop-2-enylamino)sulfonyl]phenyl ketone 41 Princeton OSSL_069057 3,5-dimethylpiperidyl 0 H H (USA) 4-(pyrazolylmethyl)phenyl ketone 42 ENAMINE T6146953 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-(1,2,4-triazolyl)phenyl ketone 43 ENAMINE T6151807 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-Imidazolylphenyl ketone 44 ENAMINE T6154154 methyl 4-[(3,5-dimethylpiperidyl) 0 H H (Ukraine) carbonyl]benzoate Chemical Molecular Sample No R³ Formula Weight 36

C₂₂H₂₆N₂O₂ 350.45 37

C₁₉H₂₂N₂O₃ 326.39 38

C₂₂H₂₇NO₃ 353.45 39

C₂₁H₂₃NO₂ 321.41 40 SO₂NHCH₂CHCH₂ C₁₇H₂₄N₂O₃S 336.45 41

C₁₈H₂₃N₃O 297.39 42

C₁₆H₂₀N₄O 284.36 43

C₁₇H₂₁N₃O 283.37 44 COOCH₃ C₁₆H₂₁NO₃ 275.34

TABLE 9 Compound Sample (Fit for the basic structure)

Sample Supplier ID No (Country) Number Name n R¹ R² 45 ENAMINE T6244948 amino-N-{4-[(3,5- 0 H H (Ukraine) dimethylpiperidyl)carbonyl] phenyl}amide 46 ENAMINE T6248261 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-{2-[(methylsulfonyl)amino]ethyl} phenyl ketone 47 OTAVA 1159464 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-(1,2,3,4-tetraazolyl)phenyl ketone 48 UOS PB184210594 3,5-dimethylpiperidyl 3-chloro- 0 OCH₃ Cl (Ukraine) 4,5-dimethoxyphenyl ketone 49 UOS PB184211566 N-{4-[(3,5-dimethylpiperidyl)carbonyl] 0 H H (Ukraine) phenyl}cyclopropylcarboxamide 50 UOS PB184211716 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-(methylsulfonyl)phenyl ketone 51 UOS PB184213202 4,5-dimethyl-3- 0 SO₂NHCH₃ CH₃ (Ukraine) [(methylamino)sulfonyl]phenyl 3,5- dimethylpiperidyl ketone 52 UOS PB184213204 3-[(dimethylamino)sulfonyl]- 0 CH₃ SO₂N(CH₃)₂ (Ukraine) 4,5-dimethylphenyl 3,5-dimethylpiperidyl ketone 53 UOS PB184213358 3,5-dimethylpiperidyl 0 H H (Ukraine) 4-pyrazolylphenyl ketone Chemical Molecular Sample No R³ Formula Weight 45 NHCONH₂ C₁₅H₂₁N₃O₂ 275.35 46 CH₂CH₂NHSO₂CH₃ C₁₇H₂₆N₂O₃S 338.46 47

C₁₅H₁₉N₅O 285.34 48 OCH₃ C₁₆H₂₂ClNO₃ 311.8 49

C₁₈H₂₄N₂O₂ 300.4 50 SO₂CH₃ C₁₅H₂₁NO₃S 295.4 51 CH₃ C₁₇H₂₆N₂O₃S 338.46 52 CH₃ C₁₈H₂₈N₂O₃S 352.49 53

C₁₇H₂₁N₃O 283.37

TABLE 10 Compound Sample (Fit for the basic structure)

Sample Supplier ID No (Country) Number Name n R¹ R² 54 UOS PB184214520 3,5-dimethylpiperidyl 0 OCH₃ OCH₃ (Ukraine) 4-bromo-3,5- dimethoxyphenyl ketone 55 Zelinsky UZI/8148542 3,5-dimethylpiperidyl 0 H H (add1) (ART- 4-[(3,5- CHEM) dimethylpiperidyl) (Germany) carbonyl]phenyl ketone 56 AsinexGold BAS 3,5-dimethylpiperidyl 0 H H (add2) (Russia) 03276131 4-(phenylsulfonyl) phenyl ketone 56 TimTec ST5271268 3,5-dimethylpiperidyl 0 H H (add2) (USA) 4-(phenylsulfonyl) phenyl ketone 57 Asinex ASN 3,5-dimethylpiperidyl 0 H H (add3) Platinum 06365831 4-{[4-(5- (Russia) methylbenzotriazolyl) piperidyl]sulfonyl} phenyl ketone 58 ENAMINE T0505- 3,5-dimethylpiperidyl 0 H NO₂ (add4) (Ukraine) 2963 3-nitro- 4-pyrrolidinyl phenyl ketone 59 (add5) ENAMINE (Ukraine) T0505- 3770 3,5-dimethylpiperidyl 4-chloro-3-{[(2- methoxyphenyl)amino] sulfonyl} phenyl ketone 0

H 60 (add6) ENAMINE (Ukraine) T0505- 7165 3,5-dimethylpiperidyl 4-bromo-3- (morpholin-4- ylsulfonyl) phenyl ketone 0 H

Chemical Molecular Sample No R³ Formula Weight 54 Br C₁₆H₂₂BrNO₃ 356.25 55 (add1)

C₂₂H₃₂N₂O₂ 356.5 56 (add2)

C₂₀H₂₃NO₃S 357.47 56 (add2)

C₂₀H₂₃NO₃S 357.47 57 (add3)

C₂₆H₃₃N₅O₃S 495.64 58 (add4)

C₁₈H₂₅N₃O₃ 331.41 59 Cl C₂₁H₂₅ClN₂O₄S 436.95 (add5) 60 Br C₁₈H₂₅BrN₂O₄S 445.37 (add6)

TABLE 11 Compound Sample (Fit for the basic structure)

Sample Supplier ID No (Country) Number Name n R¹ R² 61 (add7)  ENAMINE (Ukraine) T0505- 8410 3,5-dimethylpiperidyl 3-{[(2-methoxyphenyl)amino] sulfonyl}-4-methylphenyl ketone 0

H 62 ENAMINE T5284681 5-({4-[(3,5-dimethylpiperidyl) 0 H H (add8)  (Ukraine) carbonyl]phenyl}methylene)- 3-(4-methylphenyl)-2-thioxo-1, 3-diazolidin-4-one 63 LifeChemicals F0473- 3,5-dimethylpiperidyl 0 H H (add9)  (Ukraine) 0330 4-(2-1,2,3,4- tetrahydroisoquinolylsulfonyl) phenyl ketone 64 LifeChemicals F0715- 3,5-dimethylpiperidyl 0 H H (add10) (Ukraine) 0116 4-[(diprop-2-enylamino)sulfonyl] phenyl ketone 65 ENAMINE T5891289 3,5-dimethylpiperidyl 0 H H (add11) (Ukraine) 4-[({[3-(trifluoromethyl)phenyl] sulfonyl}amino)methyl]phenyl ketone 65 UOS PB275100560 3,5-dimethylpiperidyl 0 H H (add11) (Ukraine) 4-[({[3-(trifluoromethyl)phenyl] sulfonyl}amino)methyl]phenyl ketone 66 ENAMINE T5891312 4-{[(2,5- 0 H H (add12) (Ukraine) dimethylphenyl)sulfonyl]amino} phenyl 3,5-dimethylpiperidyl ketone 66 UOS PB275099928 4-{[(2,5- 0 H H (add12) (Ukraine) dimethylphenyl)sulfonyl]amino} phenyl 3,5-dimethylpiperidyl ketone Chemical Molecular Sample No R³ Formula Weight 61 CH₃ C₂₂H₂₈N₂O₄S 416.53 (add7)  62 (add8) 

C₂₅H₂₇N₃O₂S 433.57 63 (add9) 

C₂₃H₂₈N₂O₃S 412.55 64 (add10)

C₂₀H₂₈N₂O₃S 376.51 65 (add11)

C₂₂H₂₅F₃N₂O₃S 454.51 65 (add11)

C₂₂H₂₅F₃N₂O₃S 454.51 66 (add12)

C₂₂H₂₈N₂O₃S 400.53 66 (add12)

C₂₂H₂₈N₂O₃S 400.53

TABLE 12 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 67 ENAMINE T6178780 4-[(3,5-dimethylisoxazol- 0 H H (add13) (Ukraine) 4-yl)methoxy]phenyl 3,5-dimethylpiperidyl ketone 68 ENAMINE T5889890 3,5-dimethylpiperidyl 0 H H (add14) (Ukraine) 4-{[(3-methoxyphenyl)sulfonyl]amino} phenyl ketone 68 UOS PB275102432 3,5-dimethylpiperidyl 0 H H (add14) (Ukraine) 4-{[(3-methoxyphenyl)sulfonyl]amino} phenyl ketone 69 ENAMINE T5891044 4-({[(2,5-dimethylphenyl)sulfonyl] 0 H H (add15) (Ukraine) amino}methyl)phenyl 3,5-dimethylpiperidyl ketone 69 UOS PB275100774 4-({[(2,5-dimethylphenyl) 0 H H (add15) (Ukraine) sulfonyl]amino}methyl) phenyl 3,5-dimethylpiperidyl ketone 70 ENAMINE T5621791 N-{4-[(3,5- 0 H H (add16) (Ukraine) dimethylpiperidyl)carbonyl]phenyl}- 2-(4-oxo-2-pyrrolidinyl (1,3-thiazolin-5-yl))acetamide 71 ENAMINE T5852810 3,5-dimethylpiperidyl 0 H H (add17) (Ukraine) 4-[(4-methylpiperidyl)sulfonyl] phenyl ketone 72 ENAMINE T5885590 3,5-dimethylpiperidyl 0 H H (add18) (Ukraine) 4-[(ethylphenylamino)sulfonyl] phenyl ketone Sample Chemical Molecular No R³ Formula Weight 67 (add13)

C₂₀H₂₆N₂O₃ 342.43 68 (add14)

C₂₁H₂₆N₂O₄S 402.51 68 (add14)

C₂₁H₂₆N₂O₄S 402.51 69 (add15)

C₂₃H₃₀N₂O₃S 414.56 69 (add15)

C₂₃H₃₀N₂O₃S 414.56 70 (add16)

C₂₃H₃₀N₄O₃S 442.57 71 (add17)

C₂₀H₃₀N₂O₃S 378.53 72 (add18)

C₂₂H₂₈N₂O₃S 400.53

TABLE 13 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 72 UOS PB258783634 3,5-dimethylpiperidyl 0 H H (add18) (Ukraine) 4-[(ethylphenylamino)sulfonyl] phenyl ketone 73 Princeton OSSK_810181 3,5-dimethylpiperidyl 0 H H (add19) (USA) 4-[(4-bromopyrazolyl)methyl] phenyl ketone 74 Princeton OSSK_810279 3,5-dimethylpiperidyl 0 H H (add20) (USA) 4-[(4-bromo-3,5-dimethylpyrazolyl)methyl] phenyl ketone 75 Princeton OSSK_824836 2-{4-[((3S,5R)- 0 H H (add21) (USA) 3,5-dimethylpiperidyl)carbonyl]phenyl}- 2,4,5-trihydroisothiazole-1,1,3-trione 76 Princeton OSSK_824897 2-{4-[((3S,5R)- 0 H H (add22) (USA) 3,5-dimethylpiperidyl)carbonyl]phenyl}- 4-methyl-2,4,5-trihydroisothiazole- 1,1,3-trione 77 Princeton OSSK_824958 2-{4-[((3S,5R)-3,5- 0 H H (add23) (USA) dimethylpiperidyl)carbonyl]phenyl)- 4,4-dimethyl-2,4,5-trihydroisothiazole- 1,1,3-trione 78 ENAMINE T5891124 4-[({[4-(tert-butyl)phenyl]sulfonyl}amino) 0 H H (add24) (Ukraine) methyl]phenyl 3,5-dimethylpiperidyl ketone Sample Chemical Molecular No R³ Formula Weight 72 (add18)

C₂₂H₂₈N₂O₃S 400.53 73 (add19)

C₁₈H₂₂BrN₃O 376.29 74 (add20)

C₂₀H₂₆BrN₃O 404.34 75 (add21)

C₁₇H₂₂N₂O₄S 350.43 76 (add22)

C₁₈H₂₄N₂O₄S 364.46 77 (add23)

C₁₉H₂₆N₂O₄S 378.49 78 (add24)

C₂₅H₃₄N₂O₃S 442.61

TABLE 14 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 78 UOS PB275102704 4-[({[4-(tert- 0 H H (add24) (Ukraine) butyl)phenyl]sulfonyl} amino)methyl]phenyl 3,5- dimethylpiperidyl ketone 79 ENAMINE T5984447 4-{[(2,3- 0 H H (add25) (Ukraine) dimethylphenyl)amino] sulfonyl}phenyl 3,5- dimethylpiperidyl ketone 80 (add26) ENAMINE (Ukraine) T5991171 3,5-dimethylpiperidyl 4-methyl-3- {[(4-methylphenyl)amino] sulfonyl}phenyl ketone 0 H

81 ENAMINE T5992247 3,5-dimethylpiperidyl 0 H H (add27) (Ukraine) 4-{[(4-methylphenyl)amino] sulfonyl}phenyl ketone 81 UOS PB291309174 3,5-dimethylpiperidyl 0 H H (add27) (Ukraine) 4-{[(4-methylphenyl)amino] sulfonyl}phenyl ketone 82 ENAMINE T5993116 3,5-dimethylpiperidyl 0 H H (add28) (Ukraine) 4-{[(4-fluorophenyl)amino] sulfonyl}phenyl ketone 83 ENAMINE T5996172 3,5-dimethylpiperidyl 0 H H (add29) (Ukraine) 4-[(2-methyl(1,3-thiazol- 4-yl))methylthio] phenyl ketone 84 ENAMINE T5997889 4-[(2H,3H-benzo[3,4-e] 0 H H (add30) (Ukraine) 1,4-dioxin-6-ylsulfonyl) amino]phenyl 3,5-dimethylpiperidyl ketone 85 ENAMINE T6053107 3,5-dimethylpiperidyl 4- 0 H H (add31) (Ukraine) [(6-methyl(4-hydroimidazo [1,2-a]pyridin-2- yl))methoxy] phenyl ketone Sample Chemical Molecular No R³ Formula Weight 78 (add24)

C₂₅H₃₄N₂O₃S 442.61 79 (add25)

C₂₂H₂₈N₂O₃S 400.53 80 (add26) CH₃ C₂₂H₂₈N₂O₃S 400.53 81 (add27)

C₂₁H₂₆N₂O₃S 386.51 81 (add27)

C₂₁H₂₆N₂O₃S 386.51 82 (add28)

C₂₀H₂₃FN₂O₃S 390.47 83 (add29)

C₁₉H₂₄N₂OS₂ 360.54 84 (add30)

C₂₂H₂₆N₂O₅S 430.52 85 (add31)

C₂₃H₂₇N₃O₂ 377.48

TABLE 15 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 86 ENAMINE T6055225 3,5-dimethylpiperidyl 0 H H (add32) (Ukraine) 4-[(5-methyl(1,2,4-oxadiazol-3-yl))methoxy] phenyl ketone 87 ENAMINE T6232627 3,5-dimethylpiperidyl 0 H H (add33) (Ukraine) 4-(1,2,3,4-tetrahydroquinolylsulfonyl) phenyl ketone 88 ENAMINE T6101662 3,5-dimethylpiperidyl 0 H H (add34) (Ukraine) 4-{[(4-ethoxyphenyl)amino]sulfonyl} phenyl ketone 88 UOS PB184214142 3,5-dimethylpiperidyl 0 H H (add34) (Ukraine) 4-{[(4-ethoxyphenyl)amino]sulfonyl} phenyl ketone 89 ENAMINE T6114600 3,5-dimethylpiperidyl 0 H H (add35) (Ukraine) 4-{[(4-fluorophenyl)sulfonyl]amino} phenyl ketone 90 Princeton OSSL__069022 3,5-dimethylpiperidyl 0 H H (add36) (USA) 4-[(4-chloro-3,5-dimethylpyrazolyl)methyl] phenyl ketone 91 Zelinsky UZI/2518327 3,5-dimethylpiperidyl 0 H H (add37) (ART- 4-(5-phenyl(1,3,4-oxadiazol-2-yl)) CHEM) phenyl ketone (Germany) Sample Chemical Molecular No R³ Fomula Weight 86 (add32)

C₁₈H₂₃N₃O₃ 329.39 87 (add33)

C₂₃H₂₈N₂O₃S 412.55 88 (add34)

C₂₂H₂₈N₂O₄S 416.53 88 (add34)

C₂₂H₂₈N₂O₄S 416.53 89 (add35)

C₂₀H₂₃FN₂O₃S 390.47 90 (add36)

C₂₀H₂₆ClN₃O 359.89 91 (add37)

C₂₂H₂₃N₃O₂ 361.44

TABLE 16 Compound Sample (Fit for the basic structure)

Sample Supplier ID No (Country) Number Name n R¹ R² 92 ENAMINE T6131058 3,5-dimethylpiperidyl 0 H H (add38) (Ukraine) 4-{[(2-methoxyethyl)amino] sulfonyl}phenyl ketone 93 ENAMINE T6132785 4-(benzimidazol-2- 0 H H (add39) (Ukraine) ylthiomethyl)phenyl 3,5- dimethylpiperidyl ketone 93 UOS PB184210580 4-(benzimidazol-2- 0 H H (add39) (Ukraine) ylthiomethyl)phenyl 3,5- dimethylpiperidyl ketone 94 (add40) ENAMINE (Ukraine) T6142049 3,5-dimethylpiperidyl 4-chloro-3- [(3-methylpiperidyl)sulfonyl]phenyl ketone 0

H 95 ENAMINE T6151070 3,5-dimethylpiperidyl 0 H H (add41) (Ukraine) 4-[(phenylsulfonyl)amino] phenyl ketone 96 ENAMINE T6154735 3-{4-[(3,5- 0 H H (add42) (Ukraine) dimethylpiperidyl)carbonyl] phenyl}-2-methyl- 3-hydroquinazolin-4-one 97 ENAMINE T6182050 4-({4-[(3,5- 0 H H (add43) (Ukraine) dimethylpiperidyl)carbonyl] phenyl}sulfonyl)piperazin-2-one 98 ENAMINE T6186857 N-{4-[(3,5- 0 H H (add44) (Ukraine) dimethylpiperidyl)carbonyl] phenyl}-2-thienylcarboxamide Sample Chemical Molecular No R³ Fomula Weight 92 SO₂NHCH₂CH₂OCH₃ C₁₇H₂₆N₂O₄S 354.46 (add38) 93 (add39)

C₂₂H₂₅N₃OS 379.52 93 (add39)

C₂₂H₂₅N₃OS 379.52 94 Cl C₂₀H₂₉ClN₂O₃S 412.97 (add40) 95 (add41)

C₂₀H₂₄N₂O₃S 372.48 96 (add42)

C₂₃H₂₅N₃O₂ 375.46 97 (add43)

C₁₈H₂₅N₃O₄S 379.47 98 (add44)

C₁₉H₂₂N₂O₂S 342.46

TABLE 17 Compound Sample (Fit for the basic structure)

Sample Supplier No (Country) ID Number Name n R¹ R² 98 UOS PB184213386 N-{4-[(3,5-dimethylpiperidyl) 0 H H (add44) (Ukraine) carbonyl]phenyl}- 2-thienylcarboxamide 99 (add45) ENAMINE (Ukraine) T6190262 3,5-dimethylpiperidyl 4-methyl-3-(piperidylsulfonyl) phenyl ketone 0 H

100 ENAMINE T5768807 3,5-dimethylpiperidyl 0 H H (add46) (Ukraine) 4-(piperidylsulfonyl) phenyl ketone 100 UOS PB234963720 3,5-dimethylpiperidyl 0 H H (add46) (Ukraine) 4-(piperidylsulfonyl) phenylketone 101 LifeChemicals F0440-0309 3,5-dimethylpiperidyl 0 H H (add47) (Ukraine) 4-[(3,5-dimethylpiperidyl) sulfonyl] phenyl ketone 102 UOS PB184212112 3,5-dimethylpiperidyl 0 H H (add48) (Ukraine) 4-(4-chloro-3,5- dimethylpyrazolyl)phenyl ketone 103 (add49) UOS (Ukraine) PB184212166 3,5-dimethylpiperidyl 4-chloro-3-(piperidylsulfonyl) phenyl ketone 0 H

104 UOS PB184213526 4-benzimidazolylphenyl 0 H H (add50) (Ukraine) 3,5-dimethylpiperidyl ketone Sample Chemical Molecular No R³ Fomula Weight 98 (add44)

C₁₉H₂₂N₂O₂S 342.46 99 CH₃ C₂₀H₃₀N₂O₃S 378.53 (add45) 100 (add46)

C₁₉H₂₈N₂O₃S 364.5 100 (add46)

C₁₉H₂₈N₂O₃S 364.5 101 (add47)

C₂₁H₃₂N₂O₃S 392.56 102 (add46)

C₁₉H₂₄ClN₃O 345.87 103 Cl C₁₉H₂₇ClN₂O₃S 398.95 (add49) 104 (add50)

C₂₁H₂₃N₃O 333.43

TABLE 18 Compound Sample (Fit for the basic structure)

Sample Supplier ID No (Country) Number Name n R¹ R² 105 (add51) UOS (Ukraine) PB184214076 3,5-dimethylpiperidyl 4-chloro-3-{[(4- ethoxyphenyl)amino] sulfonyl}phenyl ketone 0

H 106 UOS PB184215230 3,5-dimethylpiperidyl 0 H H (add52) (Ukraine) 4-{[(4-fluoro-3- methylphenyl)sulfonyl]amino} phenyl ketone Sample Chemical Molecular No R³ Fomula Weight 105 Cl C₂₂H₂₇ClN₂O₄S 450.98 (add51) 106 (add52)

C₂₁H₂₅FN₂O₃S 404.5

TABLE 19 1

2

3

4

TABLE 20 5

6

7

8

TABLE 21 9

10

11

12

TABLE 22 13

14

15

16

TABLE 23 17

18

19

20

TABLE 24 21

22

23

24

25

26

TABLE 25 27

28

29

30

TABLE 26 31

32

33

34

TABLE 27 35

36

37

38

39

40

TABLE 28 41

42

43

44

45

TABLE 29 46

47

48

49

TABLE 30 50

51

52

53

TABLE 31 54

55 (add 1)

56 (add 2)

57 (add 3)

TABLE 32 58 (add 4)

59 (add 5)

60 (add 6)

61 (add 7)

TABLE 33 62 (add 8)

63 (add 9)

64 (add 10)

65 (add 11)

TABLE 34 66 (add 12)

67 (add 13)

68 (add 14)

69 (add 15)

TABLE 35 70 (add 16)

71 (add 17)

72 (add 18)

73 (add 19)

TABLE 36 74 (add 20)

75 (add 21)

76 (add 22)

77 (add 23)

78 (add 24)

TABLE 37 79 (add 25)

80 (add 26)

81 (add 27)

82 (add 28)

83 (add 29)

84 (add 30)

TABLE 38 85 (add 31)

86 (add 32)

87 (add 33)

88 (add 34)

TABLE 39 89 (add 35)

90 (add 36)

91 (add 37)

92 (add 38)

93 (add 39)

TABLE 40 94 (add 40)

95 (add 41)

96 (add 42)

97 (add 43)

TABLE 41  98 (add 44)

 99 (add 45)

100 (add 46)

101 (add 47)

TABLE 42 102 (add 48)

103 (add 49)

104 (add 50)

105 (add 51)

106 (add 52)

Specific examples of the pharmacologically acceptable salt of the compound represented by formula (I) (including formula (Ia)) include, but are not limited to, alkaline metal salts such as sodium salt, potassium salt or lithium salt; alkaline earth metal salts such as calcium salt or magnesium salt; organic amine salts such as cyclohexylamine salt, trimethylamine salt or diethanolamine salt; basic amino acid salts such as arginine salt or lysine salt; and ammonium salts.

It is possible to convert the compound represented by formula (I) (including formula (Ia)) to a pharmacologically acceptable ester according to conventional methods. The types of the “pharmacologically acceptable ester” are not particularly limited. Any type of ester may be used as long as it has the same pharmaceutical applicability as the compound represented by formula (I) and is pharmacologically acceptable.

When the compound represented by formula (I) (including formula (Ia)) has asymmetric carbon(s) within its molecule, racemic compounds and optically active compounds thereof are also included in the present invention.

Compounds represented by formula (I) (including formula (Ia)), pharmacologically acceptable salts thereof or pharmacologically acceptable esters thereof may occur as various solvates, e.g., solvates formed with water, methanol, ethanol, dimethylformamide, ethyl acetate or the like. Pharmaceutical compositions comprising such solvates are also included in the present invention.

Compounds represented by formula (I) (including formula (Ia)), pharmacologically acceptable salts thereof or pharmacologically acceptable esters thereof bind to mSin3B that specifically binds to neural restrictive silencer factor (NRSF). Therefore, they may be used as a prophylactic and/or a therapeutic for diseases associated with abnormal expression of neural restrictive silencer factor NRSF/REST or abnormal expression of genes targeted by NRSF/REST. Examples of diseases associated with abnormal expression of neural restrictive silencer factor NRSF/REST or abnormal expression of genes targeted by NRSF/REST include neurodegenerative diseases (such as Down's syndrome, Alzheimer's disease, Huntington's disease and Parkinson's disease), cancer (such as medulloblastoma), atopic dermatitis, diabetes, cardiomyopathy, neuropathic pain and so forth.

It has been described above that abnormal expression of NRSF/REST or genes targeted by NRSF/REST is involved in Down's syndrome, Alzheimer's disease, Huntington's disease, medulloblastoma and neuropathic pain.

It has been reported that gene expression of an enzyme tyrosine hydroxylase which provides a rate limiting step in the synthetic pathway of dopamine (which is believed to be depleted in Parkinson's disease patients' brains) is regulated by NRSF/REST (Regulation of human tyrosine hydroxylase gene by neuron-restrictive silencer factor. Kim S M, Yang J W, Park M J, Lee J K, Kim S U, Lee Y S, Lee M A. BBRC 346, 426 (2006); Neuroscience Research, 65-236)).

A report has been made that NRSF/REST is a repressor of the expression of neuropilin-1 that is a receptor for semaphorin 3A (Sema3A) (Neuron restrictive silencer factor NRSF/REST is a transcriptional repressor of neuropilin-1 and diminishes the ability of semaphorin 3A to inhibit keratinocyte migration. Kurschat P, Bielenberg D, Rossignol-Tallandier M, Stahl A, Klagsbrun M. J Biol Chem. 2006 Feb. 3; 281(5):2721-9. Epub 2005 Dec. 5.). It has been reported that activation of Sema3A signals is effective in alleviating symptoms of atopic dermatitis; this suggests that NRSF/REST can be a novel target molecule for treating atopic dermatitis.

It has been reported that NRSF/REST is involved in the regulation of expression of connexin36 (essential for insulin secretion) (Critical role of the transcriptional repressor neuron-restrictive silencer factor in the specific control of connexin36 in insulin-producing cell lines. Martin D, Tawadros T, Meylan L, Abderrahmani A, Condorelli D F, Waeber G, Haefliger J A. J Biol Chem. 2003 Dec. 26; 278(52):53082-9. Epub 2003 Oct. 16.). This suggests that NRSF/REST can be a novel target molecule for treating diabetes.

It has been reported that mice expressing a dominant-negative mutant of NRSF/REST in their hearts exhibit dilated cardiomyopathy and highly likely to undergo arrhythmias or sudden death (NRSF regulates the fetal cardiac gene program and maintains normal cardiac structure and function. K. Kuwahara, Y. Saito, M. Takano, Y. Arai, S. Yasuno, Y. Nakagawa, N. Takahashi, Y. Adachi, G. Takemura, M. Horie, Y. Miyamaoto, T. Morisaki, S. kuratomi, A. Noma, H. Fujiwara, Y. Yoshimasa, H. Kinoshita, R. Kawakami, I. Kishimoto, M. Nakanishi, S. Usami, Y. Saito, M. Harada, K. Nakao, The EMBO Journal, 22, 6310-6321 (2003)). This suggests that NRSF/REST can be a novel target molecule for treating cardiomyopathy.

A substance capable of binding to the PAH1 domain of mSin3B (e.g., compounds represented by formula (I) (including formula (Ia)), pharmacologically acceptable salts thereof or pharmacologically acceptable esters thereof) may be administered to a human or an animal in the form of a pharmaceutical preparation (e.g., injection, capsules, tablets, powder, granules, etc.) formulated by conventional methods. For example, such a pharmaceutical preparation may be administered orally at a daily dose of approximately 0.1-1000 mg/kg (body weight), preferably at a daily dose of approximately 1-500 mg/kg (body weight), as converted to the amount of the active ingredient. This dose may be administered once or may be divided into several times. However, the dose and the number of times of administration may be appropriately altered depending on the symptoms and age of the patient, the method of administration route, and so forth. When the substance is formulated into an injection, a carrier such as physiological saline may be used. When the substance is formulated into capsules, tablets, powder or granules, excipients such as starch, lactose, sucrose or calcium carbonate; binders such as starch paste, gum arabic, gelatin, sodium alginate, carboxymethylcellulose or hydroxypropylcellulose; lubricants such as magnesium stearate or talc; and disintegrants such as starch, agar, crystalline cellulose, calcium carbonate, sodium hydrogencarbonate or sodium alginate may be used. The content of the active ingredient in pharmaceutical preparations may be varied between 1 to 99% by weight. For example, when the pharmaceutical preparation takes the form of tablets, capsules, granules or powder, the content of the active ingredient is preferably 5-80% by weight; when the pharmaceutical preparation takes the form of injection, the content of the active ingredient is preferably 1-10% by weight.

EXAMPLES

Hereinbelow, the present invention will be described with reference to the following Examples. However, the present invention is not limited to these Examples.

In Preparation Examples 1 to 22, the derivatives of 3,5-dimethyl-1-(3-methyl-4-nitrobenzoyl)piperidine shown below were synthesized.

Methods of synthesis are summarized in Schemes 1 to 4 described below.

Preparation Example 1 Scheme 1 Preparation of 3,5-Dimethyl-1-(3-Methylbenzoyl)piperidine (NCR-1)

3,5-Dimethylpiperidine (0.73 g) and triethylamine (2.25 ml) were dissolved in dichloromethane (20 ml). A solution of 3-methylbenzoylchloride (1.00 g) in dichloromethane (10 ml) was added dropwise at the freezing point. After stirring for 30 minutes at 0° C., the reaction solution was poured into water (100 ml) and extracted with chloroform (50 ml). The organic layer was washed with saturated brine (100 ml), dried over anhydrous sodium sulfate and, after filtration, concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography (developing solvent: n-hexane/ethyl acetate=4:1) to obtain the subject compound (NCR-1 cis form:trans form=9:1) (0.95 g, yield 63%) as a colorless oil. ¹H-NMR (CDCl₃, 500 MHz, δ; ppm) 0.76-1.86 (10H, m), 2.15-2.23 (0.9H, m), 2.36 (3H, s), 2.44-2.49 (0.9H, m), 3.08 (0.1H, m), 3.20 (0.1H, m), 3.32-3.34 (0.1H, m), 3.63-3.65 (0.9H, m), 7.14 (1H, d, J=7.3 Hz), 7.19 (1H, d, J=7.3 Hz), 7.20 (1H, s), 7.26 (1H, t, J=7.6 Hz); MS (EI) m/z: 231 (M⁺).

Preparation Example 2 Scheme 1 Preparation of 3,5-Dimethyl-1-(4-Nitrobenzoyl)piperidine (NCR-2)

The subject compound (NCR-2 cis form:trans form=9:1) (yield 92%) was obtained in the same manner as in Preparation Example 1 except that 4-nitrobenzoylchloride was used instead of 3-methylbenzoylchloride. Crude crystals of NCR-2 (1.31 g) were re-crystallized from n-hexane-chloroform to obtain white crystals (0.78 g).

mp 120-125° C.; ¹H-NMR (CDCl₃, 500 MHz, δ; ppm) 0.77-1.71 (10H, m), 2.20-2.51 (0.9H, m), 2.51-2.56 (0.9H, m), 2.99 (0.1H, m), 3.22 (0.1H, m), 3.27-3.29 (0.1H, m), 3.42-3.45 (0.9H, m), 3.89-3.91 (0.1H, m), 4.66-4.68 (0.9H, m), 7.54 (2H, d, J=8.7 Hz), 8.27 (2H, d, J=8.7 Hz); MS (EI) m/z: 262 (M⁺); Anal. Calcd. for C₁₄H₁₈N₂O₃: C, 64.10; H, 6.92; N, 10.68. Found: C, 65.51; H, 7.17; N, 10.97.

Preparation Example 3 Scheme 1 Preparation of 3-Methyl-1-(4-Nitrobenzoyl)piperidine (NCR-4)

The subject compound (NCR-4) (yield 89%) was obtained in the same manner as in Preparation Example 1 except that 3-methylpiperidine was used instead of 3,5-dimethylpiperidine and that 4-nitrobenzoylchloride was used instead of 3-methylbenzoylchloride. Crude crystals of NCR-4 (1.19 g) were re-crystallized from n-hexane-chloroform to obtain brown crystals (0.83 g).

mp 70.2-71.3° C.; ¹H-NMR (CDCl₃, 500 MHz, δ; ppm) 0.79 (1.5H, d, J=6.5 Hz), 0.97 (1.5H, d, J=6.5 Hz), 1.17-1.89 (5H, m), 2.47 (0.5H, m), 2.67 (0.5H, m), 2.84 (0.5H, m), 2.96 (0.5H, m), 3.42 (0.5H, m), 3.49 (0.5H, m), 4.51 (1H, m), 7.54 (2H, d, J=8.8 Hz), 8.25 (2H, d, J=8.5 Hz); MS (EI) m/z: 248 (M⁺); Anal. Calcd. for C₁₃H₁₆N₂O₃: C, 62.89; H, 6.50; N, 11.28. Found: C, 62.78; H, 6.42; N, 11.28.

Preparation Example 4 Scheme 1 Preparation of 3-Methyl-1-(3-Methylbenzoyl)piperidine (NCR-5)

The subject compound (NCR-4) (yield 75%) was obtained as a colorless, oily material, in the same manner as in Preparation Example 1 except that 3-methylpiperidine was used instead of 3,5-dimethylpiperidine.

¹H-NMR (CDCl₃, 500 MHz, δ; ppm) 0.77 (1.5H, s), 0.94 (1.5H, s), 1.11-1.85 (51H, m), 2.34 (3H, m), 2.41 (0.5H, m), 2.61 (0.5H, m), 2.78 (0.5H, m), 2.90 (0.5H, m), 3.57-3.65 (1H, m), 4.51 (1H, m), 7.13 (1H, d, J=7.4 Hz), 7.17-7.18 (2H, m), 7.24 (1H, t, J=7.8 Hz); MS (EI) m/z: 217 (M⁺).

Preparation Example 5 Scheme 1 Preparation of 1-(Benzoyl)-3,5-Dimethyl piperidine (NCR-6)

The subject compound (NCR-6 cis form:trans form=9:1) (yield 76%) was obtained in the same manner as in Preparation Example 1 except that benzoylchloride was used instead of 3-methylbenzoylchloride. Crude crystals of NCR-6 (1.18 g) were re-crystallized from n-hexane-chloroform to obtain white crystals (0.48 g).

mp 107.2-108.7° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 0.76-0.96 (6H, m), 1.47-1.87 (4H, m), 2.17-2.22 (0.9H, m), 2.45-2.50 (0.9H, m), 3.07 (0.1H, m), 3.21 (0.1H, m), 3.32-3.34 (0.1H, m), 3.61-3.63 (0.9H, m), 3.88 (0.1H, m), 4.68-4.70 (0.9H, m), 7.36-7.41 (5H, m); MS (EI) m/z: 217 (M⁺); Anal. Calcd. for C₁₄H₁₉NO: C, 77.38; H, 8.81; N, 6.45. Found: C, 77.03; H, 8.72; N, 6.59.

Preparation Example 6 Scheme 1 Preparation of 1-Benzoylpiperidine (NCR-10)

The subject compound (NCR-10) (yield 76%) was obtained as a colorless oil in the same manner as in Preparation Example 1 except that piperidine was used instead of 3,5-dimethylpiperidine and that benzoylchloride was used instead of 3-methylbenzoylchloride.

¹H-NMR (CDCl3, 500 MHz, δ; ppm) 1.41 (2H, s), 1.57 (4H, s), 3.24 (2H, s), 3.62 (2H, s), 7.29 (5H, s); MS (EI) m/z: 189 (M⁺),

Preparation Example 7 Scheme 1 Preparation of 3,5-Dimethyl-1-(4-Chlorobenzoyl)piperidine (NCR-11)

The subject compound (NCR-11 cis form:trans form=9:1) (yield 77%) was obtained in the same manner as in Preparation Example 1 except that 4-chlorobenzoylchloride was used instead of 3-methylbenzoylchloride. Crude crystals of NCR-11 (1.11 g) were re-crystallized from n-hexane-chloroform to obtain white crystals (0.53 g).

mp 113.5-115.4° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 0.74-0.93 (7H, m), 1.45-1.96 (3H, m), 2.14-2.19 (0.9H, m), 2.45-2.50 (0.9H, m), 3.03 (0.1H, m), 3.17 (0.1H, m), 3.28 (0.1H, m), 3.54-3.56 (0.9H, m), 3.83 (0.1H, m), 4.62-4.64 (0.9H, m), 7.28-7.32 (2H, m), 7.33-7.36 (2H, m); MS (EI) m/z: 251 (M⁺); Anal. Calcd. for C₁₄H₁₈NO: C, 66.79; H, 7.21; N, 5.56. Found: C, 66.42; H, 6.96; N, 5.80.

Preparation Example 8 Scheme 2 Preparation of 3-Methyl-1-(3-Methyl-4-Nitrobenzoyl)piperidine (NCR-3)

3-Methyl-4-nitrobenzoic acid (1.00 g) and N,N-dimethylformamide (catalytic amount) were dissolved in dichloromethane (20 ml). Oxalyl chloride (0.94 ml) was added, and the resultant mixture was stirred at 0° C. for 1 hour and 30 minutes. The reaction solution was concentrated under reduced pressure, dissolved in dichloromethane (10 ml) and added dropwise to a solution of 3-methylpiperidine (1.10 g) and triethylamine (1.90 ml) in dichloromethane (20 ml) at the freezing point. After stirring for 20 hours at 0° C., the reaction solution was poured to water (100 ml) and extracted with chloroform (50 ml). The organic layer was washed with saturated brine (100 ml), dried over anhydrous sodium sulfate and, after filtration, concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography (developing solvent: n-hexane/ethyl acetate=2:1) to obtain the subject compound (NCR-3) (1.37 g, yield 94%). Crude crystals of NCR-3 (1.37 g) were re-crystallized from n-hexane-chloroform to obtain white crystals (0.88 g).

mp 82.0-82.8° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 0.72 (1.5H, d, J=6.5 Hz), 0.89 (1.5H, d, J=6.5 Hz), 1.08-1.80 (5H, m), 2.34-2.39 (0.5H, m), 2.53 (3H, s), 2.55-2.60 (0.5H, m), 2.72-2.76 (0.5H, m), 2.84-2.89 (0.5H, m), 3.35-3.38 (0.5H, m), 3.42-3.45 (0.5H, m), 4.42-4.44 (1H, m), 7.22 (1H, d, J=8.3 Hz), 7.26 (1H, s), 7.90 (1H, d, J=8.3 Hz); MS (EI) m/z: 262 (M⁺); Anal. Calcd. for C₁₄H₁₈N₂O₃: C, 64.10; H, 6.92; N, 10.68. Found: C, 65.23; H, 7.13; N, 10.96.

Preparation Example 9 Scheme 2 Preparation of 1-(3-Methyl-4-Nitrobenzoyl)piperidine (NCR-8)

The subject compound (NCR-8) (yield 89%) was obtained in the same manner as in Preparation Example 8 except that piperidine was used instead of 3-methylpiperidine. Crude crystals of NCR-8 (1.22 g) were re-crystallized from n-hexane-chloroform to obtain white crystals (0.98 g).

mp 71.7-72.2° C.; ¹H-NMR (CDCl₃, 500 MHz; ppm) 1.52 (2H, s), 1.69 (4H, s), 2.61 (3H, s), 3.29 (2H, s), 3.71 (2H, s), 7.33 (1H, d, J=8.3 Hz), 7.36 (1H, s), 7.99 (1H, d, J=8.4 Hz); MS (EI) m/z: 248 (M⁺); Anal. Calcd. for C₁₃H₁₆N₂O₃: C, 62.89; H, 6.50; N, 11.28. Found: C, 62.29; H, 6.40; N, 11.17.

Preparation Example 10 Scheme 2 Preparation of N,N-Diethyl-3 Methyl-4-Nitrobenzamide (NCR-9)

The subject compound (NCR-9) (yield 71%) was obtained in the same manner as in Preparation Example 8 except that diethylamine was used instead of 3-methylpiperidine. Crude crystals of NCR-9 (0.93 g) were re-crystallized with n-hexane-chloroform to obtain brown crystals (0.63 g).

mp 74.5-76.0° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 1.13 (3H, m), 1.26 (3H, m), 2.63 (3H, s), 3.24 (2H, m), 3.36 (2H, m), 7.34-7.37 (2H, m), 8.01 (1H, d, J=8.0 Hz); MS (EI) m/z: 236 (M⁺); Anal. Calcd. for C₁₂H₁₆N₂O₃: C, 61.00; H, 6.83; N, 11.86. Found: C, 60.72; H, 6.94; N, 11.83.

Preparation Example 11 Scheme 2 Preparation of 3-Methyl-4-Nitro-N,N-Dipropylbenzamide (NCR-13)

The subject compound (NCR-13) (yield 90%) was obtained as a yellow oil in the same manner as in Preparation Example 8 except that dipropylamine was used instead of 3-methylpiperidine.

¹H-NMR (CDCl3, 500 MHz, δ; ppm) 0.58-0.61 (3H, m), 0.79-0.82 (3H, m), 1.35-1.39 (2H, m), 1.42-1.57 (2H, s), 2.45 (3H, s), 2.97-3.00 (2H, m), 3.29-3.32 (2H, m), 7.17 (1H, d, J=8.4 Hz), 7.19 (1H, s), 7.83 (1H, d, J=8.3 Hz); MS (EI) m/z: 264 (MI).

Preparation Example 12 Scheme 2 Preparation of N,N-Diisobutyl-3-Methyl-4-Nitrobenzamide (NCR-14)

The subject compound (NCR-14) (yield 99%) was obtained as a yellow oil in the same manner as in Preparation Example 8 except that diisobutylamine was used instead of 3-methylpiperidine.

¹H-NMR (CDCl3, 500 MHz, δ; ppm) 0.65 (6H, d, J=6.5 Hz), 0.88 (6H, d, J=7.0 Hz), 1.75-1.81 (1H, m), 2.01-2.05 (1H, m), 2.51 (3H, s), 2.96 (2H, d, J=7.5 Hz), 3.27 (2H, d, J=7.5 Hz), 7.20-7.22 (2H, m), 7.89 (1H, d, J=9.0 Hz); MS (EI) m/z: 292 (M⁺).

Preparation Example 13 Scheme 2 Preparation of N,N-Diisopropyl-3-Methyl-4-Nitrobenzamide (NCR-15)

The subject compound (NCR-15) (yield 71%) was obtained as a yellow oil in the same manner as in Preparation Example 8 except that diisopropylamine was used instead of 3-methylpiperidine. Crude crystals of NCR-15 (0.94 g) were re-crystallized from n-hexane-chloroform to obtain white crystals (0.60 g).

mp 107.6-109.7° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 1.16 (6H, m), 1.54 (6H, m), 3.54 (1H, m), 3.71 (1H, m), 7.26 (1H, d, J=8.3 Hz), 7.28 (1H, s), 8.00 (1H, d, J=8.3 Hz); MS (EI) m/z: 264 (M⁺); Anal. Calcd. for C₁₄H₂₀N₂O₃: C, 63.62; H, 7.63; N, 10.60. Found: C, 63.47; H, 7.47; N, 10.66.

Preparation Example 14 Scheme 2 Preparation of N,N-di-sec-Butyl-3-Methyl-4-Nitrobenzamide (NCR-16)

The subject compound (NCR-16) (yield 83%) was obtained as a yellow oil in the same manner as in Preparation Example 8 except that di-sec-butylamine was used instead of 3-methylpiperidine.

¹H-NMR (CDCl3, 500 MHz, δ; ppm) 0.83-0.86 (3H, m), 0.95-0.98 (3H, m), 1.16-1.17 (3H, m), 1.43 (1H, m), 1.50-1.53 (3H, m), 1.58-1.60 (1H, m), 1.85-2.28 (2H, m), 2.62 (3H, s), 3.15 (1H, m), 3.46 (1H, m), 7.26-7.28 (2H, m), 7.99 (1H, d, J=8.2 Hz); MS (EI) m/z: 292 (M⁺).

Preparation Example 15 Scheme 2 Preparation of 2,6-Dimethyl-1-(3-Methyl-4-Nitrobenzoyl)piperidine (NCR-17)

The subject compound (NCR-17) (yield 82%) was obtained in the same manner as in Preparation Example 8 except that cis-2,6-dimethylpiperidine was used instead of 3-methylpiperidine. Crude crystals of NCR-17 (1.14 g) were re-crystallized from n-hexane-chloroform to obtain white crystals (0.79 g).

mp 99.7-100.5° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 1.29 (6H, m), 1.55-1.74 (6H, m), 1.84-1.89 (2H, m), 7.30 (1H, d, J=8.3 Hz), 7.31 (1H, s), 8.01 (1H, d, J=8.3 Hz); MS (EI) m/z: 276 (M⁺); Anal. Calcd. for C₁₅H₂₀N₂O₃: C, 65.20; H, 7.30; N, 10.14. Found: C, 64.97; H, 7.01; N, 10.07.

Preparation Example 16 Scheme 2 Preparation of N,N-Dibenzyl-3-Methyl-4-Nitrobenzamide (NCR-18)

The subject compound (NCR-18) (yield 75%) was obtained as white crystals in the same manner as in Preparation Example 8 except that dibenzylamine was used instead of 3-methylpiperidine and that re-crystallization with n-hexane-chloroform was carried out instead of silica gel flash column chromatography.

mp 105.8-108.7° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 2.58 (3H, s), 4.35 (2H, s), 4.72 (2H, s), 7.12 (2H, d, J=7.0 Hz), 7.29-7.43 (10H, m), 7.96 (1H, d, J=8.5 Hz); MS (EI) m/z: 360 (M⁺); Anal. Calcd. for C₂₂H₂₀N₂O₃: C, 73.32; H, 5.59; N, 7.77. Found: C, 73.10; H, 5.95; N, 8.08.

Preparation Example 17 Scheme 2 Preparation of 1-(3-Methyl-4-Nitrobenzoyl)pyrrolidine (NCR-19)

The subject compound (NCR-19) (yield 96%) was obtained in the same manner as in Preparation Example 8 except that pyrrolidine was used instead of 3-methylpiperidine. Crude crystals of NCR-19 (1.13 g) were re-crystallized from n-hexane-chloroform to obtain yellow crystals (0.71 g).

mp 61.3-61.9° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 1.87-1.91 (2H, m), 1.93-1.97 (2H, m), 2.58 (3H, s), 3.35 (2H, t, J=6.7 Hz), 3.61 (2H, t, J=7.0 Hz), 7.42 (1H, d, J=8.3 Hz), 7.46 (1H, s), 7.96 (1H, d, J=8.4 Hz); MS (EI) m/z: 234 (M⁺); Anal. Calcd. for C₁₂H₁₄N₂O₃: C, 61.53; H, 6.02; N, 11.96. Found: C, 61.41; H, 5.98; N, 11.92.

Preparation Example 18 Scheme 2 Preparation of 1-(3-Methyl-4-Nitrobenzyol)azepane (NCR-20)

The subject compound (NCR-20) (yield 92%) was obtained in the same manner as in Preparation Example 8 except that azepane was used instead of 3-methylpiperidine. Crude crystals of NCR-20 (1.21 g) were re-crystallized from n-hexane-chloroform to obtain yellow crystals (0.69 g).

mp 62.5-63.8° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 1.62-1.65 (6H, m), 1.82-1.85 (2H, m), 2.62 (3H, s), 3.36 (2H, t, J=5.5 Hz), 3.68 (2H, t, J=5.5 Hz), 7.36 (1H, d, J=8.2 Hz), 7.38 (1H, s), 8.00 (1H, d, J=8.3 Hz); MS (EI) m/z: 262 (M⁺); Anal. Calcd. for C₁₄H₁₈N₂O₃: C, 64.10; H, 6.92; N, 10.68. Found: C, 63.84; H, 6.76; N, 10.70.

Preparation Example 19 Scheme 2 Preparation of 1-(3-Methyl-4-Nitrobenzyol)azocane (NCR-21)

The subject compound (NCR-21) (yield 64%) was obtained in the same manner as in Preparation Example 8 except that azocane was used instead of 3-methylpiperidine. Crude crystals of NCR-21 (0.89 g) were re-crystallized from n-hexane-chloroform to obtain yellow crystals (0.80 g).

mp 75.7-77.0° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 1.59 (8H, m), 1.85-1.86 (2H, m), 2.60 (3H, s), 3.26 (2H, m), 3.61 (2H, t, J=6.5 Hz), 7.30 (1H, d, J=8.5 Hz), 7.31 (1H, s), 7.98 (1H, d, J=8.3 Hz); MS (EI) m/z: 276 (M⁺); Anal. Calcd. for C₁₅H₂₀N₂O₃: C, 65.20; H, 7.30; N, 10.14.

Found: C, 65.09; H, 7.29; N, 10.10.

Preparation Example 20 Scheme 2 Preparation of N-Cyclohexyl-3-Methyl-4-Nitrobenzamide (NCR-22)

The subject compound (NCR-22) (yield 53%) was obtained in the same manner as in Preparation Example 8 except that cyclohexylamine was used instead of 3-methylpiperidine. Crude crystals of NCR-22 (0.70 g) were re-crystallized with n-hexane-chloroform to obtain white crystals (0.55 g).

mp 134.2-141.0° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 1.20-1.29 (3H, m), 1.40-1.48 (21H, m), 1.66-1.80 (3H, m), 2.04-2.05 (2H, m), 2.64 (3H, s), 3.96-3.99 (1H, m), 5.95 (1H, brs), 7.66 (1H, d, J=8.5 Hz), 7.73 (1H, s), 7.99 (1H, d, J=8.6 Hz); MS (EI) m/z: 262 (M⁺); Anal. Calcd. for C₁₄H₁₈N₂O₃: C, 64.10; H, 6.92; N, 10.68. Found: C, 63.89; H, 6.72; N, 10.68.

Preparation Example 21 Scheme 3 Preparation of 3,5-Dimethyl-1-(3-Methyl-4-Nitrobenzyl)piperidine (NCR-7)

3-Methyl-4-nitrobenzyl bromide (1.00 g), 3,5-dimethylpiperidine (0.60 ml) and potassium carbonate (0.90 g) were dissolved in acetone (20 ml), followed by heating under reflux for 6 hours. The reaction solution was concentrated under reduced pressure, dissolved in chloroform (10 ml), poured into water (100 ml) and extracted with chloroform (50 ml). The organic layer was washed with saturated brine (100 ml), dried over anhydrous sodium sulfate and, after filtration, concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography (developing solvent: n-hexane/ethyl acetate=10:1) to obtain the subject compound (NCR-7) (0.70 g, yield 61%) as a yellow oil.

¹H-NMR (CDCl₃, 500 MHz, δ; ppm) 0.80-0.82 (6H, m), 1.44-1.48 (2H, m), 1.64-1.72 (3H, m), 2.59 (3H, s), 2.71-2.74 (2H, m), 3.46 (2H, s), 7.27-7.29 (2H, m), 7.92 (1H, d, J=9.0 Hz); MS (EI) m/z: 262 (M⁺);

Preparation Example 22 Scheme 4 Preparation of 3,5-Dimethyl-1-[(3-Methyl-4-Nitrophenyl)sulfonyl]piperidine (NCR-12) Step 1: Preparation of 3-Methyl 4-Nitrobenzenethiol (1)

5-Chloro-2-nitrotoluene (1.00 g), sodium sulfate nonahydrate (1.01 g), sulfur (136.24 mg) and sodium hydroxide (233.12 mg) were dissolved in ethanol (20 ml) and heated under reflux for 2 hours. The reaction solution was poured into 10% hydrochloric acid (100 ml) and extracted with ethyl acetate (50 ml). The organic layer was washed with saturated brine (100 ml), dried over anhydrous sodium sulfate and, after filtration, concentrated under reduced pressure.

The residue was purified by silica gel flash column chromatography (developing solvent: n-hexane/ethyl acetate=15:1) to obtain the subject compound (1) (0.74 g, yield 75%) as brown crystals.

¹H-NMR (DMSO, 500 MHz, δ; ppm) 2.01 (1H, s), 2.48 (3H, s), 7.50-7.63 (2H, m), 7.99 (1H, s).

Step 2: Preparation of 3-Methyl-4-Nitrobenzenesulfonic Acid (2)

The 3-methyl 4-nitrobenzenethiol (1) (0.74 g) obtained in the preceding step was dissolved in acetic acid (10 ml). Aqueous hydrogen peroxide (5 ml) was added thereto, and the resultant mixture was stirred at room temperature for 1 hour and 30 minutes. The reaction solution was concentrated under reduced pressure, purified by silica gel flash column chromatography (developing solvent: n-hexane/ethyl acetate=20:1) to obtain the subject compound (2) (0.64 g, yield 68%) as a yellow oil.

¹H-NMR (DMSO, 500 MHz, δ; ppm) 2.56 (3H, s), 7.78 (1H, d, =8.1 Hz), 7.83 (1H, s), 7.96 (1H, d, J=8.4 Hz).

Step 3: Preparation of 3,5-Dimethyl-1-[(3-Methyl-4-Nitrophenyl)sulfonyl]piperidine

The 3-methyl-4-nitrobenzenesulfonic acid (2) (0.64 g) obtained in Step 2 was dissolved in thionyl chloride (1.2 ml) and heated under reflux for 20 hours. The reaction solution was concentrated under reduced pressure and dissolved in dichloromethane (5 ml). This solution was added dropwise to a solution of 3,5-dimethylpiperidine (0.49 ml) and triethylamine (1.20 ml) in dichloromethane (10 ml) at the freezing point. After stirring for 3 hours and 30 minutes at room temperature, the reaction solution was poured into water (50 ml) and extracted with chloroform (20 ml). The organic layer was washed with saturated brine (50 ml), dried over anhydrous sodium sulfate and, after filtration, concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography (developing solvent: n-hexane/ethyl acetate=10:1) to obtain the subject compound (NCR-12) (155.3 mg, yield 17%). Crude crystals of NCR-12 (155.3 mg) were re-crystallized from n-hexane-chloroform to obtain brown crystals (99.2 mg).

mp 132.7-138.5° C.; ¹H-NMR (CDCl3, 500 MHz, δ; ppm) 0.88-0.89 (6H, m), 1.58-1.81 (6H, m), 3.76 (2H, d, J=6.5 Hz), 7.73 (1H, d, J=8.0 Hz), 7.75 (1H, s), 8.06 (1H, d, J=8.3 Hz); MS (EI) m/z: 312 (M⁺); Anal. Calcd. for C₁₄H₂₀N₂O₄S: C, 53.83; H, 6.45; N, 8.97. Found: C, 53.62; H, 6.49; N, 9.11.

Example 1

Experiments were carried out under the following STD-NMR measuring conditions.

1. Samples

-   -   (1) Protein: ¹⁵N-mSin3B [According to the method described in         Example 1 in WO2006/030722, ¹⁵N-mSin3B (the PAH1 domain of         mSin3B (a.a. 28-107) labeled with ¹⁵N) was prepared.]     -   (2) Ligands: 3,5-dimethylpeperidyl 3-methyl-4-nitrophenyl ketone         (purchased from SPECS);         1-[4-(difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one         (purchased from Enamine); 3,5-dimethylpiperidyl         4-chloro-3-nitrophenyl ketone (purchased from Vitas-M         Laboratory, LTD.), 3,5-dimethylpiperidyl 4-fluorophenyl ketone         (purchased from Vitas-M Laboratory, LTD.),         2-(2,6-dimethylmorpholin-4-yl)-N-(2-chloro-4-fluorophenyl)acetamide         (purchased from Enamine); 1-benzoyl-3,5-dimethylpiperidine         (NCR6) (prepared in Preparation Example 5);         3,5-dimethyl-1-(3-methyl-4-nitrobenzyl)piperidine (NCR7)         (prepared in Preparation Example 21);         3,5-dimethyl-1-(4-chlorobenzoyl)piperidine (NCR11) (prepared in         Preparation Example 7); 3-methyl-4-nitro-N,N-dipropylbenzamide         (NCR13) (prepared in Preparation Example 11);         N,N-diisobutyl-3-methyl-4-nitrobenzamide (NCR14) (prepared in         Preparation Example 12);         N,N-diisopropyl-3-methyl-4-nitrobenzamide (NCR15) (prepared in         Preparation Example 13)         2. Sample Preparation     -   (1) Samples necessary for measurement were prepared in 500 μl         samples.     -   (2) The concentration of the protein was 10 μM, and the         concentration of the ligands was 400 μM.     -   (3) As a solvent, 100 mM phosphate buffer (pH 7.2) (5% d-DMSO)         was used. The protein and the ligand were mixed therein.         3. NMR Measuring Conditions         1H-STD; number of scans: 4; measurement time: 2 minutes         4. NMR Apparatus         Bruker AVANCE 600 MHz (cryo-probe), Bruker AVANCE 700 MHz         (cryo-probe)

The results are shown in FIGS. 1 to 11. Since STD spectra were observed with the 11 ligands used in the measurement, it was judged that these ligands interact with the protein.

Example 2

Cell growth effects were examined on 3,5-dimethylpiperidyl 3-methyl-4-nitrophenyl ketone (compound 155) and 1-[4-(difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one (compound A28) (MTT assay using a human medulloblastoma cell strain).

Materials and Methods

Compounds: 3,5-dimethylpiperidyl 3-methyl-4-nitrophenyl ketone (compound 155) (purchased from SPECS); 1-[4-(difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one (compound A28) (purchased from Enamine)

Cell: DAOY (human medulloblastoma cell strain) (provided by Kanno, Department of Neurosurgery, School of Medicine, Yokohama City University)

Medium: DMEM (High Glucose, Nacalai Tesque)

Reagent for cell counting: MTT cell counting kit (Nacalai Tesque) MTT Assay: (operations)

Day −1: DAOY was plated on three 96-well plates at 5×10³ cells/well. These three plates were for use on day 0, day 1 and day 3, respectively. As a medium, 10% FBS-containing DMEM was used.

Day 0: MTT assay was carried out using the plate for day 0 to measure the activity at the basal cell count. With respect to the plates for day 1 and day 3, the compound was added to give a concentration of 100 μg/ml (as controls, DMEM alone and DMEM containing DMSO (solvent) were used). Specifically, the compound-containing DMEM was prepared in advance, and the compound was added to the plate through medium exchange. At this time, FBS concentration was lowered to 5% in order to prevent the masking of the compound's effect due to excessive growth signals. Day 1: MTT assay was carried out using the plate for day 1. Day 3: MTT assay was carried out using the plate for day 3. Data Analysis: Relative growths on day 1 and day 3 were calculated, with the average of MTT activities (Ab 570 nm) on day 0 in the rows of wells for addition of the respective compounds being taken, as 100.

Each experiment was performed in quadruple and each run was repeated three times. Relative values based on the values of day 0 were used to calculate data for n=12 wells and statistical tests were performed.

Test was by t-test between the cell count with DMEM alone and the cell count with the compound or DMSO.

MIT Assay: A technique for cell counting using the respiratory activity of mitochondria as an indicator. When the respiratory activity is high (the value at Ab 570 nm is high), it can be interpreted that the cell count is large.

Results

The results are summarized in the following Table.

TABLE 43 Relative Growth DMEM + Compound 155 A28 DMSO DMEM only Day 100.00 ± 5.08  100.00 ± 6.56 100.00 ± 3.76  100.00 ± 5.45  0 Day 123.16 ± 10.03 233.28 ± 1.69 158.33 ± 15.78 146.33 ± 11.22 1 Day 105.07 ± 17.53  90.17 ± 171 297.78 ± 15.42 282.09 ± 15.63 3 Test (Two Sample t-Test) (Compound) or (DMEM + DMSO) vs (DMEM only) Compound 155 A28 DMEM + DMSO Day 1 0.12215 5.90E−08 0.52411 Day 3 7.71E−08 1.23E−11 0.46362 Compound A28: This compound showed a transient, abnormal cell growth on Day 1. When cells were observed on day 3, they appeared morphologically dead. It is believed that cells finally die from depletion of nutrients in the medium or the like as a result of abnormally accelerated growth. The phenotype of this compound was very distinct even without performing MTT assay. Compound 155: Cell growth was inhibited on both day 1 and day 3. It seems that this compound is the most promising as a drug candidate.

Example 3 Materials and Methods

Compounds: No. 5, No. 15, No. 23, NCR 6, NCR 7, NCR 11, NCR 13, NCR 14, NCR 15

Cell: DAOY (human medulloblastoma cell strain)

Medium: DMEM (High Glucose, Nacalai Tesque)

Reagent for cell counting: MTT cell counting kit (Nacalai Tesque) *Hereinafter, referred to as MTT assay.

Operations

Day −1:

DAOY was plated on three 96-well plates at 5×10³ cells/well. These three plates were for use on day 0, day 1 and day 3, respectively. As a medium, 10% FBS-containing DMEM was used.

Day 0:

The medium in the plate for day 0 was exchanged with 5% FBS-containing DMEM, and cells were cultured therein for 30 minutes. Then, MTT assay was carried out to measure the activity at the basal cell count.

With respect to the plates for day 1 and day 3, the medium was exchanged with 5% FBS-containing medium, and the compound was added simultaneously at this time (as a control, DMSO (the solvent) alone was added).

Day 1:

MTT assay was carried out using the plate for day 1.

Day 3:

MTT assay was carried out using the plate for day 3.

Data Analysis:

Relative growths on day 1 and day 3 were calculated, with the average of MTT activities (Ab 570 nm) on day in the rows of wells for the respective compounds being taken as 100. Each experiment was performed in quadruple.

Statistical test was performed by compound-treated cells and DMSO-treated cells.

Results

Compounds No. 5, No. 15 and No. 23 were added to cells at final concentrations of 100 μg/ml, 10 μg/ml, 1 μg/ml and 0.1 μg/ml, and the relative growth rates of the cells were examined. With any of the compounds, measured values of MTT assay showed a significant decrease, compared to DMSO-added cells, when the concentration was 100 μg/ml. With compound No. 5, measured values of MTT assay did not change greatly during the experiment period; therefore, this compound is likely to have an inhibitory action on cell growth. On the other hand, with compounds No. 15 and No. 23, almost all cells had died three days after their addition. Therefore, it was suggested that these compounds have cytotoxicity (FIG. 12).

Compounds NCR 6, NCR 7, NCR 11, NCR 13, NCR 14 and NCR 15 were added at a final concentration of 200 μM/ml or 20 μM/ml. When NCR 7 was added at 200 μM/ml, cytotoxicity was observed (FIG. 13).

Example 4 Evaluation of Efficacies of mSin3B Compounds on Chronic Pain Model Animal

A neuropathic pain model was created by partial sciatic nerve ligation using 6-10 week old C57BL male mice (20-25 g) (TEXAM Corporation) (Inoue et al., Nature Medicine, 10: 712-718, 2004). mSin3B compounds were dissolved in 100% DMSO. Immediately before administration, the compound was diluted with artificial cerebrospinal fluid (DMSO final concentration: 0.5%) and administered into the spinal subarachnoid space (i.t.) at 0.5 nmol/5 μl. For control group, DMSO (0.5%) diluted with artificial cerebrospinal fluid was administered as a vehicle. In an experiment involving systemic administration of mSin3B compounds, the compound was diluted with physiological saline (DMSO final concentration: 10%) immediately before administration and administered at 5 mg/kg intraperitoneally (i.p.). For the control group in this experiment, DMSO (10%) diluted with physiological saline was administered as a vehicle. On the other hand, morphine was dissolved in physiological saline and administered intraplantarly (i.pl.) at 30 nmol/20 μl. ACU values from 10 to 60 minutes after morphine administration were calculated to evaluate of the analgesic effect of morphine. For behavioral analysis concerning pain, (1) “electrical stimulation-induced paw withdrawal (EPW) test” (Matsumoto et al., J Pharmacol Exp Ther, 318:735-740, 2006; Ueda, Mol Pain, 4:11, 2008, REVIEW) to evaluate a pain threshold in response to C-fiber specific electrical stimulation (5 Hz) and (2) “thermal paw withdrawal test” (Inoue et al., Nature Medicine, 10: 712-718, 2004) to evaluate a pain threshold in response to thermal stimulation were used. For expression analysis of a group of pain-associated genes (Na_(v) 1.8 and MOP), the cell soma of primary sensory neuron (dorsal root ganglia) after nerve injury was used; evaluation was made by quantitative real time PCR.

mSin3B compounds: 3,5-dimethylpiperidyl 3-methyl-4-nitrophenyl ketone (compound 155), 1-[4-(difluoromethoxy)phenyl]-2-(3,5-dimethylpiperidyl)ethan-1-one (compound A28), N-[(4-fluorophenyl)methyl]-N′-(3-methylbutyl)butane-1,4-diamide (compound 106)

Results and Discussion Experiment (1)

Three days after nerve injury, mSin3B compound (A28) was administered once, followed by analysis of mRNA levels of a group of pain-associated genes (Na_(v) 1.8 and MOP) in dorsal root ganglia at 3, 6 and 12 hours after the administration (n=3 for each analysis). As a result, a tendency was observed that the lowering of expression of Na_(v) 1.8 and MOP after nerve injury is recovered by about 10-15% by treatment with A28 (0.5 nmol i.t.) (FIG. 14). It was suggested that about 3-6 hours are needed for the effect to appear.

Experiment (2)

Subsequently, the efficacies of mSin3B compounds (A28, 155, 106 (NC)) on hypoesthesia after nerve injury were evaluated by EPW test. Three days after nerve injury, increase of pain threshold in response to C-fiber stimulation (i.e., hypoesthesia) was observed in injury groups (injury-veh group: n=5; injury-A28 group: n=6; injury-155 group: n=6; injury-106 group: n=6) compared to control group (sham-veh group: n=6). Further, mSin3B compounds (A28, 155, 106 (NC)) or vehicle was administered once per day after behavioral analysis. As a result, a tendency of recovery from hypoesthesia was observed starting 4 days after nerve injury (1 day after the start of administration) in injury-A28 group and injury-155 group; this tendency became more marked 5 days after nerve injury (2 days after the start of administration) (FIG. 15). As a result of statistical analysis, a significant difference was recognized between pain threshold values at 3 days after nerve injury and 5 days after nerve injury in injury-A28 group and injury-155 group. On the other hand, no effect on pain threshold was recognized in injury-106 group.

Experiment (3)

Subsequently, in consideration of clinical indications, mSin3B compound (A28 or 155) was administered systemically (intraperitoneally) (5 mg/kg) and consecutively for 3, 4 and 5 days after nerve injury, followed by evaluation of the effect on pain threshold. Pain tests were performed prior to administration of the compound. As a result, time-dependent recovery from hypoesthesia was observed in both A28- and 155-administered groups (n=3 for each group) relative to the hypoesthesia at 3 days after nerve injury (control group) (FIG. 16).

Experiment (4)

Further, efficacies of mSinB3 compounds (A28, 155, 106 (NC)) on morphine resistance after nerve injury were evaluated using thermal paw withdrawal test. Administration of mSin3B compounds was started 3 days after nerve injury, and after 5 days after nerve injury 2 days after the start of administration, peripheral morphine (30 nmol i.pl.) analgesia was analyzed (sham-veh group: n=6; injury-veh group: n=5; injury-A28 group: n=6; injury-155 group: n=6; injury-106 group: n=3). The results revealed that, compared to sham-veh group, effect of morphine analgesia disappeared in injury-veh group, but morphine analgesia almost equivalent to that in sham-veh group was obtained in injury-A28 group. In injury-155 group, significant recovery of morphine analgesia was recognized. On the other hand, morphine analgesia was hardly recognized in injury-106 group. These results are shown in FIG. 17.

Experiment (5)

mRNA levels of Na_(v) 1.8 in dorsal root ganglia after administration of mSin3B compound (A28 or 155) (0.5 nmol i.t.) were evaluated by a quantitative real time method, revealing that compound 155 exhibited a remarkable inhibitory effect on the lowering of expression of Na_(v) 1.8 due to nerve injury; however, A28 did not exhibit a significant change (sham-veh group: n=3; injury-veh group: n=3; injury-A28 group: n=3; injury-155 group: n=2) (FIG. 18).

All the publications, patents and patent applications cited herein are incorporated herein by reference in their entirety.

INDUSTRIAL APPLICABILITY

A substance capable of binding to the PAH1 domain of mSin3B (e.g., a compound represented by formula (I), pharmacologically acceptable salt thereof, or pharmacologically acceptable ester thereof) may be used as a medicine, especially as a prophylactic and/or a therapeutic for diseases associated with abnormal expression of neural restrictive silencer factor NRSF/REST or abnormal expression of genes targeted by NRSF/REST.

PRIOR ART LITERATURE Patent Documents

-   Patent Document No. 1: WO2006/030722 International Publication

Non-Patent Documents

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The invention claimed is:
 1. A method of treating a disease associated with abnormal expression of neural restrictive silencer factor NRSF/REST or abnormal expression of genes targeted by NRSF/REST, comprising administering to a subject a pharmacologically effective amount of a substance capable of binding to the PAH1 domain of mSin3B, wherein the disease is neuropathic pain and the substance is a compound represented by A28 or 155 or a pharmacological acceptable salt or ester thereof, where A28 and 155 are:


2. A method of preparing and administering a substance capable of binding to the PAH1 domain of mSin3B, comprising: preparing a prophylactic and/or a therapeutic substance that binds to the PAH1 domain of mSin3B for a disease associated with abnormal expression of neural restrictive silencer factor NRSF/REST or abnormal expression of genes targeted by NRSF/REST; and administering to a subject the substance that binds to the PAH1 domain of mSin3B, wherein the disease is neuropathic pain and the substance is a compound represented by A28 or 155 or a pharmacological acceptable salt or ester thereof, where A28 and 155 are:


3. A method of treatment with a substance capable of binding to the PAH1 domain of mSin3B, comprising: administering to a subject a substance capable of binding to the PAH1 domain of mSin3B to treat a disease associated with abnormal expression of neural restrictive silencer factor NRSF/REST or abnormal expression of genes targeted by NRSF/REST, wherein the disease is neuropathic pain and the substance is a compound represented by A28 or 155 or a pharmacological acceptable salt or ester thereof, where A28 and 155 are: 